基于EFDC和WASP模型的突发水污染事故影响的预测预警

近年来,我国突发水污染事故频发。长江作为我国最重要的水源地,其水质安全受到沿江众多化工企业可能突发污染事故的威胁。因此,开展南京化工园突发水污染事故影响的预测预警研究意义重大。基于EFDC和WASP模型,建立了南京化工园突发水污染事故影响的预测模型,并以龙翔甲苯罐区泄漏为例进行了事故情景模拟。研究表明：所建的预测模型能够对南京化工园突发水污染事故后污染物的水环境行为进行快速的模拟和预测,并且能够在地理信息系统的图层上以动画的形式实时展示事故影响的范围和程度,可以为南京化工园突发水污染事故的预警应急提供决策依据;基于EFDC构建的二维水动力模型能够较为准确地反映研究区的水动力情况;事故情景中排放的甲苯在研究江段能够较快地稀释扩散,挥发作用对甲苯的衰减过程影响显著,平水期比枯水期更有利于水体中甲苯的衰减     

河流近域土地利用格局与水质相关性分析——以巢湖流域为例

以河流近域土地利用构成与水环境质量间定量关系为研究对象,基于巢湖流域40个水质监测断面和320个河流近域作用区,运用GIS空间分析功能计算不同尺度作用区内土地利用构成,借助相关分析、冗余分析(RDA)等数理统计手段,分析土地利用构成与水质指数间的相关关系;并分析和比较了流域内山区和平原地区土地利用构成与水质之间关系。结果表明,巢湖流域近河道地区土地利用构成对各水质指数有重要影响,且受地形因素影响。其中,建设用地对河流水质恶化具有明显作用;河流沿岸林地布局能显著改善水质,尤其是对氨氮和高锰酸盐指数敏感;耕地面积变化与水质相关性不显著。RDA冗余分析证实了不同尺度下的土地利用类型对水环境影响具有尺度效应。研究成果对巢湖流域水环境管理具有重要的实际指导意义,并为同类研究提供借鉴     

Salting-out phenomenon and 1-octanol/water partition coefficient of metalaxyl pesticide

In this paper, we present the effect of inorganic cations such as Na⁺, K⁺, Ca²⁺, Mg²⁺ on the salting-out phenomenon of metalaxyl from pure water to aqueous salt solutions. Moreover the 1-octanol/water partition coefficient in pure water is presented. To accomplish this, aqueous solubility of metalaxyl was determined in pure water, in different salt solution (NaCl, KCl, CaCl₂ and MgCl₂), and at different concentration level ranging from 0.01 to 1.5 M. The 1-octanol/water partition coefficient was determined using the static shake-flask method. Solubility was determined using dynamic saturation method for pure water in the range of 298.15-325.15 K and at 298.15 K for different salt solutions. The solubility value in pure water for studied interval was found constant (m = 3.118 × 10⁻² mol kg⁻¹).Solubility values were used to calculate the standard molar Gibbs free energy of dissolution (Δ_solG°) and transfer (Δ_trG°) at 298.15 K. The values of Δ_trG° from pure to all studied aqueous salt solutions did not exceed 2 kJ mol⁻¹, the value of Δ_solG° of dissolution is 18.5 ±0.72 kJ mol⁻¹. The 1-octanol/water partition coefficient in pure water log K_o/w is equal to 1.69. The obtained results confirm the classification of the neutral metalaxyl as a slightly hydrophobic molecule.     

Enhanced retention of linuron, alachlor and metalaxyl in sandy soil columns intercalated with wood barriers

A study has been made of the effect a reactive barrier made of pine (softwood) or oak (hardwood) wood intercalated in a sandy soil column has on the retention of linuron, alachlor and metalaxyl (pesticides with contrasting physicochemical characteristics). The leaching of pesticides has been carried out under a saturated flow regime and breakthrough curves (BTCs) have been obtained at flow rates of 1 mL min⁻¹ (all pesticides) and 3 mL min⁻¹ (linuron). The cumulative curves in the unmodified soil indicate a leaching of pesticides >80% of the total amount of compound added. After barrier intercalation, linuron leaching decreases significantly and a modification of the leaching kinetics of alachlor and metalaxyl has been observed. The theoretical R factors increased ∼2.6-3.3, 1.2-1.6-fold, and 1.4-1.7-fold and the concentration of the maximum peak decreased ∼6-12-fold, 2-4-fold and 1.2-2-fold for linuron, alachlor and metalaxyl, respectively. When considering the three pesticides, significant correlations have been found between the theoretical retardation factor (R) and the pore volume corresponding to the maximum peaks of the BTCs (r = 0.77; p < 0.05) or the total volume leached (r = −0.78; p < 0.05). The results reveal the efficacy of reactive wood barriers to decrease the leaching of pesticides from point sources of pollution depends on the type of wood, the hydrophobicity of the pesticide and the adopted water flow rate. Pine was more effective than oak in decreasing the leaching of hydrophobic pesticide linuron or in decreasing the maximum peak concentration of the less hydrophobic pesticides in soils. Efficacy of these wood barriers was limited for the least hydrophobic pesticide metalaxyl.     

Zero-valent iron nanoparticles in treatment of acid mine water from in situ uranium leaching

Acid mine water from in situ chemical leaching of uranium (Straz pod Ralskem, Czech Republic) was treated in laboratory scale experiments by zero-valent iron nanoparticles (nZVI). For the first time, nZVI were applied for the treatment of the real acid water system containing the miscellaneous mixture of pollutants, where the various removal mechanisms occur simultaneously. Toxicity of the treated saline acid water is caused by major contaminants represented by aluminum and sulphates in a high concentration, as well as by microcontaminants like As, Be, Cd, Cr, Cu, Ni, U, V, and Zn. Laboratory batch experiments proved a significant decrease in concentrations of all the monitored pollutants due to an increase in pH and a decrease in oxidation-reduction potential related to an application of nZVI. The assumed mechanisms of contaminants removal include precipitation of cations in a lower oxidation state, precipitation caused by a simple pH increase and co-precipitation with the formed iron oxyhydroxides. The possibility to control the reaction kinetics through the nature of the surface stabilizing shell (polymer vs. FeO nanolayer) is discussed as an important practical aspect.     

Transport of chlorinated dioxins and furans in soil columns: modeling pentachlorophenol pole-treating oil influence

Column experiments were conducted to validate a screening model predicting the influence of pentachlorophenol (PCP) pole-treating oil on the vertical migration of its impurities, chlorinated dioxins and furans (PCDD/Fs). PCP pole-treating oil (15 mL d⁻¹) and water (20 mL d⁻¹) were added daily to the top of sand and organic soil columns during 35 d. Column soil samples were analyzed to determine concentrations of hydrocarbons and PCDD/Fs at several depths in the columns (0-30 cm) and their evolution in time (7, 14, 21 and 35 d).The model predicted a significant vertical migration of PCDD/Fs due to the presence of oil as a free phase and PCDD/Fs were found in the different column layers at concentrations consistent with model predictions (same order of magnitude). Measured PCDD/Fs concentrations are in total disagreement with literature data and with model prediction in the absence of oil free phase, which implies PCDD/F properties alone cannot be used to predict their fate in the current context: the influence of PCP pole-treating oil must be accounted for to properly explain their migration.     

Spatial and seasonal variations in atrazine and metolachlor surface water concentrations in Ontario (Canada) using ELISA

Concerns regarding the impacts of pesticides on aquatic species and drinking water sources have increased demands on water quality monitoring programs; however the costs of sample analysis can be prohibitive. In this study we investigated enzyme-linked immunosorbent assay (ELISA) as a cost-effective, high through-put method for measuring pesticide concentrations in surface waters. Seven hundred and thirty-nine samples from 158 locations throughout Ontario were analysed for atrazine and metolachlor from April to October 2007. Concentrations ranged from <0.1 to 3.91 μg L⁻¹ (median = 0.12 μg L⁻¹) for atrazine and from <0.1 to 1.83 μg L⁻¹ (median = 0.09 μg L⁻¹) for metolachlor. Peak concentrations occurred in late spring/early summer, in rural agricultural locations, and decreased over the remainder of the growing season for both herbicides. About 3% of the samples that had ELISA results occurring above the limit of quantification (0.10 μg L⁻¹) were evaluated against gas chromatography-mass spectrometry (GC-MS). Linear regression analysis revealed a R² value of 0.88 and 0.39, for atrazine and metolachlor, respectively. ELISA tended to overestimate concentrations for atrazine and metolachlor, most likely because the ELISA kits also detect their metabolites. Atrazine data suggest that ELISA may be used complementary with GC-MS analysis to enhance the spatial and temporal resolution of a water quality monitoring study. The commercially available metolachlor ELISA kit requires further investigation. ELISA may be used to detect atrazine and metolachlor in surface water samples, but it is not recommended as a quantitative replacement for traditional analytical methods.     

社会产品价格对水价的敏感性——基于虚拟水贸易框架的分析

虚拟水贸易是缺水地区从社会经济系统层面解决水资源短缺问题的一种策略选择,但由于长期的低水价,致使很多国家和地区的现实经济模式与虚拟水贸易战略的预期相悖.文章基于水资源投入产出分析方法,构建虚拟水贸易理论框架下的水价敏感性模型,分析水价上涨对各产业产品价格带来的影响.模型结果显示,区域水价提升对各产业产品价格的影响不仅在于该产业直接用水成本的上升,同时也不得不承受其他产业成本上升带来的间接影响,并且这两种影响作用是累加的.宁夏数据的实证得出,水价上涨对农业产品价格的影响最为强烈,批发和零售贸易餐饮业次之,对服务业产品价格的影响最弱.因此,可通过制定合理的水价调整策略,激励水资源极度缺乏的地区实施虚拟水贸易战略,避免过分强调传统的重农发展模式,促进产业结构向先进制造业和服务业转变,实现有限水资源更为合理的利用模式,达到经济发展与水生态的和谐局面.     

中国水权配置效率分析

基于整个社会的视角,对水权交易效率进行公理化分析,为水权交易的深入研究奠定基础.首先,提出分析的假设条件,定义水权配置效率,该效率满足完备性、传递性公理.其次,定义水权边际价值、总价值,提出水权边际价值递减规律.再次,给出水权配置的帕累托最优定义,提出帕累托最优时水权配置状态的定理,并论证水权的帕累托配置是稳定的水权配置状态.根据极限理论,给出水权配置序列收敛于帕累托最优配置的定义,论证了在现实水权信息不对称的情况下,只有通过水权交易重新配置水权才能逼近水权配置的最优状态--帕累托配置,而依靠行政配置无法实现.最后,采用本文理论分析我国水权交易现状,指出由于我国目前水权交易成本过高,水权配置向帕累托逼近的速度慢,水权配置无法达到帕累托最优.随着我国水权交易制度的日趋完善,水权配置将达到帕累托最优,从而实现水资源的充分利用.