Temperature-dependent sorption of polycyclic aromatic hydrocarbons on natural and treated sediments

In aqueous environment temperature is considered to play a significant role in the sorption process of polycyclic aromatic hydrocarbons (PAHs) and its influence on the sorption equilibrium is indicative of sorption energies and mechanisms. In this study, sorptions of five PAHs on three heterogeneous sorbents including one river sediment (YHR), one estuary sediment (YRD) and one treated sediment with organic matter removed (IM) were carried out at a range of temperature from 5 °C to 35 °C. Stronger sorptions were observed at lower temperatures, with the equilibrium sorption coefficient K_d increasing 2-5 times as the temperature decreases 30 °C. The increase of K_d value was attributed primarily to the change of PAH water solubility, which predicted 40-75% of the increase of K_d in the sorption process. To provide insight into the sorption mechanism, enthalpy change (ΔH_S) for the sorption process was calculated and the values were observed to be negative for all of the interactions, suggesting that the exothermal sorption of PAHs inversely dependents on temperature. Based on the values of ΔH_S, van der Waals forces were inferred as the main sorption mechanism for the PAHs, especially on the YHR sediment which contained more organic matter. For sorption of larger size PAHs on the sorbents with low organic matter, specific interactions were deduced to contribute to the overall sorption.     

水力条件对复合人工湿地处理城市受污染河水效果的影响

通过对水力负荷、水力停留时间等水力条件的控制,观察其对复合垂直上行流人工湿地处理城市受污染河水效果的影响.一年多来的运行结果表明:水力条件对复合垂直上行流人工湿地去除其他污染物的影响显著,但对总氮去除的影响不大.水力停留时间的延长可提高总磷、氨氮、COD的去除效果;随着水力负荷的增加,总磷、氨氮、COD去除率都有所增加...     

Field controlled experiments of mercury accumulation in crops from air and soil

Field open top chambers (OTCs) and soil mercury (Hg) enriched experiments were employed to study the influence of Hg concentrations in air and soil on the Hg accumulation in the organs of maize (Zea mays L.) and wheat (Triticum aestivum L.). Results showed that Hg concentrations in foliages were correlated significantly (p < 0.05) with air Hg concentrations but insignificantly correlated with soil Hg concentrations, indicating that Hg in crop foliages was mainly from air. Hg concentrations in roots were generally correlated with soil Hg concentrations (p < 0.05) but insignificantly correlated with air Hg concentrations, indicating that Hg in crop roots was mainly from soil. No significant correlations were found between Hg concentrations in stems and those in air and soil. However, Hg concentrations in upper stems were usually higher than those in bottom stems, implying air Hg might have stronger influence than soil Hg on stem Hg accumulation.     

树脂吸附-Fenton 试剂氧化法预处理炼油碱渣废水

采用树脂吸附-Fenton 试剂氧化组合工艺对某炼油企业炼油碱渣废水进行预处理.实验确定的最佳工艺条件为:3 种树脂串联吸附,废水流量0.33 mL/ min,H2O2加入量0.20 mol / L,n（H2O2）1 n（Fe2 +）= 12,Fenton 试剂氧化进水pH 3,Fenton 试剂氧化反应时间120 m...     

重金属元素在冻土与融土中迁移的对比试验

随着寒区经济的发展,冻土地区的矿山开采活动不断加剧,随之产生的重金属污染问题也越来越严重.冻土地区生态环境脆弱,一旦受到破坏就很难恢复.针对此问题,室内模拟了尾矿矿渣在冻土与融土中的填埋及其对填埋场周边土体的影响,通过检测填埋场各处土壤的温度、含水量以及重金属元素的含量,发现温度和水分对重金属元素的迁移影响很大.土壤温度越低,重金属元素的迁移越慢;在温度梯度的作用下,重金属元素均随着水分从土体的暖端向冷端迁徙并聚集于冻结锋面.重金属元素在冻土中的迁移比融土中慢,表明冻土环境不利于重金属元素的迁移.在土壤质地、温度和含水量等相同的情况下,Zn的迁移性较强,Pb和Cu的迁移性相对较弱.     

衡水市空气主要污染物体积质量的时间分布特征

利用衡水市环境监测站2005—2007年度大气例行检测的数据,对衡水市大气中主要污染物SO^2、NO^2、PM10体积质量值的逐日数据进行统计分析,得出了衡水市空气污染的现状和时间变化规律：（1）污染物体积质量值的月变化曲线呈槽型分布,非取暖期的空气状况明显好于取暖期,取暖期SO^2平均体积质量是非取暖期的2．45倍;（2）污染物体积质量值的日变化曲线基本为两高两低型,其中取暖期污染指数早晨出现极高值的时间比非取暖期明显偏晚;（3）污染物体积质量值的年变化表明了SO^2的体积质量在降低,而NO^2的体积质量却有了小幅增长。     

Size-fractionation and characterization of landfill leachate and the improvement of Cu2+ adsorption capacity in soil and aged refuse

Leachate was collected from an anaerobic lagoon at Shanghai Laogang refuse landfill, the largest landfill in China, and the sample was separated into six fractions using micro-filtration membranes, followed by ultra-filtration membranes. Several parameters of the samples were measured, including chemical oxygen demand (COD), total organic carbon (TOC), total solids (TS), pH, total phosphate (TP), total nitrogen (TN), fixed solids (FS), NH4+, orthophosphate, color, turbidity, and conductivity. These parameters were then quantitatively correlated with the molecular weight cutoff of the membrane used. Organic matter in the dissolved fraction (MW<1kDa) predominated in the leachate, accounting for 65% of TOC. Thermal infrared spectroscopy was used to characterize the filter residues. Asymmetric and symmetric stretching of methyl and methylene groups, and of functional groups containing nitrogen and oxygen atoms, were observed. In addition, the ability of two different samples to adsorb heavy metals was tested. Cu2+ was chosen as the representative heavy metal in this study, and the samples were soil; aged refuse, which had spent 8 years in a conventional sanitary landfill; and samples of soil and aged refuse treated for 48h with leachate in the ratio of 5g of sample per 50ml of leachate. Cu2+ uptake by the raw soil was approximately 4.60microg/g, while uptake by the leachate-contacted soil and leachate-contacted aged refuse were 5.66 and 5.11microg/g, respectively. These results show that the organic matter in the leachate enhanced the capacity of aqueous solutions to adsorb Cu2+.     

活性碳纤维改性技术研究进展

介绍了活性碳纤维(ACF)的孔结构及表面官能团,综述了国内外ACF改性技术的研究现状.ACF的改性主要包括孔结构调控和表面化学改性,表面化学改性包括氧化还原法、表面负载法、浸渍法、热处理法、远程等离子体处理法、微波辐照法等,也可将多种方法结合来对ACF进行改性,以改善和提高ACF的吸附性能.在总结现有研究的基础上,对ACF改性技术发展趋势进行了展望.     

Remobilization of polycyclic aromatic hydrocarbons during the resuspension of Yangtze River sediments using a particle entrainment simulator

Remobilization of 16 polycyclic aromatic hydrocarbons (PAHs) during sediment resuspension was investigated using a particle entrainment simulator at shear stress from 0.2 to 0.5Nm(-2), typical of the energy levels present in many tidally driven aquatic environments. The results suggested that desorption from the entrained particles was the primary source of dissolved PAHs. summation operatorPAHs concentrations in particles on volume normalization increased about four times. However, on mass weight basis, summation operatorPAHs concentrations decreased from 6039.74+/-138.28microgkg(-1) to 1665.39+/-112.26microgkg(-1). The same trend was observed for individual PAHs. Dissolved concentrations of PAHs demonstrated significant differences depending on molecular weight and applied shear. The distribution of PAHs between particle and water phase suggested that for three-ring PAHs, the amounts of PAHs in particles were higher than the predicted values during our experiments. This might be due to presence of another active sorbent.