退化滨水景观带植物群落生态修复技术研究进展

滨水带是重要的生态交错带,物质、养分和能量流动速率高,具有较高的生态、经济和美学价值。近年来,由于缺乏科学合理的生态规划意识,我国滨水带多被建成近直立人工护岸,加之自然、人为干扰力度的加强,滨水岸线生境破坏,生物群落丧失,滨水带退化,水岸生态环境日趋恶化。通过对滨水带生态景观功能分析,研究滨水带退化原因与机理,系统归纳了国内外退化滨水景观带植物群落生态修复相关技术的研究现状,深入探讨了生境恢复、生物廊道恢复、景观格局美化和水岸生态系统结构与功能优化等方面的研究内容,并提出今后滨水带生态修复技术研究方向,以及基于生态学、景观学、水力学、土力学、生物学、经济学等多学科背景的滨水景观带植物群落定量分析、配置方法。最后指出,滨水景观带植物群落生态修复技术研究需进一步分析我国水岸生态系统退化机理、细化滨水深槽-浅滩序列、量化滨水植被配置宽度与生物多样性关系、深化稳定化长效管理技术等,为我国退化滨水生态景观带植物群落生态修复集成技术的研究与实践提供参考,以全面有效的提高生态环境质量。     

番茄对污染土壤中邻苯二甲酸酯的吸收累积特征

利用盆栽实验研究了番茄对污染土壤中邻苯二甲酸酯(PAEs)的吸收积累特征。结果表明,番茄根系、茎、叶和果实均可以吸收累积PAEs化合物,其含量与土壤污染程度成正相关;相同处理的番茄茎、叶和果实中邻苯二甲酸正丁酯(DBP)含量均高于邻苯二甲酸异辛酯(DEHP),而番茄根系中DBP的含量低于DEHP; 4个不同处理方式土壤中DBP和DEHP的残留量顺序均为:灭菌土壤组灭菌土壤种植番茄苗组未灭菌土壤组未灭菌土壤种植番茄苗组。无论是灭菌处理还是未灭菌处理,有番茄苗组土壤中PAEs含量均低于无番茄苗组,未灭菌土壤种植番茄苗组土壤中PAEs残留量最低,PAEs削减率高达96.39%,有番茄苗组微生物数量大于无番茄苗组。这些说明土壤中PAEs的削减是番茄植物和微生物协同作用的结果。     

Effect of co-existing organic compounds on adsorption of perfluorinated compounds onto carbon nanotubes

Co-existing organic compounds may affect the adsorption of perfluorinated compounds (PFCs) and carbon nanotubes in aquatic environments. Adsorption of perfluorooctane sulfonate (PFOS), perfluorooctane acid (PFOA), perfluorobutane sulfonate (PFBS), and perfluorohexane sulfonate (PFH_xS) on the pristine multi-walled carbon nanotubes (MWCNTs-Pri), carboxyl functionalized MWCNTs (MWCTNs-COOH), and hydroxyl functionalized MWCNTs (MWCNTs-OH) in the presence of humic acid, 1-naphthol, phenol, and benzoic acid was studied. Adsorption kinetics of PFOS was described well by the pseudo-second-order model and the sorption equilibrium was almost reached within 24 h. The effect of co-existing organic compounds on PFOS adsorption followed the decreasing order of humic acid>1-naphthol>benzoic acid>phenol. Adsorbed amounts of PFOS decreased significantly in the presence of co-existing or preloaded humic acid, and both adsorption energy and effective adsorption sites on the three MWCNTs decreased, resulting in the decrease of PFOS adsorption. With increasing pH, PFOS removal by three MWCNTs decreased in the presence of humic acid and phenol. The adsorbed amounts of different PFCs on the MWCNTs increased in the order of PFBSxS相似文献   

我国新兴污染物环境风险评价与控制研究进展

目前环境化学研究热点逐渐从传统污染物转向新兴污染物,如持久性有机污染物(POPs)、环境内分泌干扰物(EDCs)、药品和个人护理品(PPCPs)等.环境中痕量新兴污染物往往会造成较高的危害和风险,日益引起广泛关注.应对新兴污染物环境问题,首先要了解其环境风险,然后进行风险控制和防范.我国新兴污染物的研究正在逐渐兴起.近年来,研究人员在我国新兴污染物环境风险评价和控制方面积极开展工作,本文综述我国这方面的研究进展,以期为进一步开展其风险防范研究提供参考.     

Removal of pharmaceutical and personal care products by sequential ultraviolet and ozonation process in a full-scale wastewater treatment plant

The application of appropriate advanced treat- ment process in the municipal wastewater treatment plants （WWTPs） has become an important issue considering the elimination of emerging contaminants, such as pharma- ceutical and personal care products （PPCPs）. In the present study, the removal of 13 PPCPs belonging to different therapeutic classes by the sequential ultraviolet （UV） and ozonation process in a full-scale WWTP in Beijing was investigated over the course of ten months. Most of the target PPCPs were effectively removed, and the median removal efficiencies of individual PPCPs, ranging from -13% to 89%, were dependent on their reaction rate constants with molecular ozone. Noticeable fluctuation in the removal efficiencies of the same PPCPs was observed in different sampling campaigns. Nevertheless, the sequential UV and ozonation process still made a significant contribution to the total elimination of most PPCPs in the full-scale WWTP, by compensating for the poor or fluctuant removal performance of PPCPs by biologic treatment process.     

电凝聚—电气浮法处理活性黄印染废水

采用电凝聚—电气浮法处理活性黄模拟印染废水。实验结果表明,在正负极换向周期为6s、电解时间为50min、搅拌转速为1 000r/min、极板间距为1.0cm、电解电压为11V、硫酸钠溶液浓度为0.010mol/L的条件下,模拟废水脱色率和COD去除率可达96%和83%以上。     

三维电极法处理钻井废水影响因素分析

采取电化学法处理某钻井废水,考察了三维电极系统处理钻井废水时,废水浓度、电流密度、处理时间、电解质浓度和pH值对废水COD降解率的影响,实验结果表明,三维电极法处理钻井废水效果显著;增大电流密度、提高电解质浓度和延长处理时间能使COD去除率提高;最佳pH值为9。正交实验得到最优水平组合为A2B3C2D3E4,在此条件下COD去除率为86.56%。     

去除水中全氟辛基磺酸的纳米吸附剂的制备及性能表征

实验研究了去除水中全氟辛基磺酸(PFOS)的纳米吸附剂的制备方法,并对其性能进行表征.研究结果表明:单体(4-乙烯基吡啶)含量对吸附剂去除PFOS的效果影响显著;而聚合状态、聚合液含水率、有机溶剂和交联剂的种类仅对吸附剂形态和比表面积有一定影响,但对吸附剂去除PFOS的效果影响不大.红外光谱揭示了单体和交联剂的有效聚合,ζ电位的测定则证实了单体和PFOS是由于静电作用而结合.     

Influence of pesticides contamination on the emission of PCDD/PCDF to the land from open burning of corn straws

Open burning of crop residues has been identified as an important emission source of PCDD/PCDF to the environment. This paper presents the first known data on the emission of PCDD/PCDF to the land considering the influence of pesticides applied in crops planting. Emission factor for PCDD/PCDF to the land from open burning of corn straw with pesticides contamination ranged from 0.07 to 0.57 ng WHO₂₀₀₅-TEQ/kg straw burned with a mean value of 0.24 ng WHO₂₀₀₅-TEQ/kg straw burned and median value of 0.20 ng WHO₂₀₀₅-TEQ/kg straw burned, respectively. The concentration was 35 to 270 times higher than that without additional pesticide contaminated. Initial observation was that emission factor for PCDD/PCDF from open burning of crop residues was overestimated in the former UNEP Dioxin Toolkit. Pesticides contamination should be considered in some hotpots where special and over dosed pesticides has been sprayed especially in developing countries.     

The lack of microbial degradation of polycyclic aromatic hydrocarbons from coal-rich soils

Analytical techniques used to assess the environmental risk of contamination from polycyclic aromatic hydrocarbons (PAHs) typically consider only abiotic sample parameters. Supercritical fluid extraction and sorption enthalpy experiments previously suggested slow desorption rates for PAH compounds in two coal-contaminated floodplain soils. In this study, the actual PAH availability for aerobic soil microorganisms was tested in two series of soil-slurry experiments. The experimental conditions supported microbial degradation of phenanthrene if it was weakly sorbed onto silica gel. Native coals and coal-derived particles in two soils effectively acted as very strong sorbents and prevented microbial PAH degradation. The long history of PAH exposure and degree of coal contamination apparently had no influence on the capability of the microbial soil community to overcome constraints of PAH availability. Within the context of the experimental conditions and the compounds chosen, our results confirm that coal-bound PAHs are not bioavailable and hence of low environmental concern.