Seasonal and spatial distribution of nonylphenol in Lanzhou Reach of Yellow River in China

Nonylphenol (NP) is known as an endocrine disruptor and consequently has drawn much environmental concern. This study focused on seasonal variation and spatial distribution of NP in various matrices including water, suspended particles, and sediment taken from Lanzhou Reach of Yellow River in China. NP was measured in July and November in 2004. Concentrations of NP in water ranged from 34.2 to 599.0 ng/l, in suspended particles from 49.6 to 2835.2 ng/g dry wt, and in sediment from 38.4 to 863.0 ng/g dry wt. In terms of most water and suspended particles samples, concentrations were higher in warmer seasons than in colder seasons. Good linear correlations (R(2)=0.90 in July, R(2)=0.97 in November) were obtained for NP concentrations between water and suspended particles. In terms of sediment samples, concentrations were higher in November than in July, probably due to greater deposition of suspended particles. Reasonable linear correlations (R(2)=0.60 in July, R(2)=0.79 in November) were obtained for NP concentrations between water and sediment.     

Application of a level IV fugacity model to simulate the long-term fate of hexachlorocyclohexane isomers in the lower reach of Yellow River basin, China

A level IV multimedia fugacity model was established to simulate the fate and transfer of hexachlorocyclohexane (HCH) isomers in the lower reach of the Yellow River basin, China, during 1952-2010. The predicted concentrations of HCHs are in good agreement with the observed ones, as indicated by the residual errors being generally lower than 0.5 logarithmic units. The effects of extensive agricultural application and subsequent prohibition of HCHs are reflected by the temporal variation of HCHs predicted by the model. It is predicted that only 1.8 tons of HCHs will be left in 2010, less than 0.06% of the highest contents (in 1983) in the study area, and about 99% of HCHs remain in soil. The proportions of HCH isomers in the environment also changed with time due to their different physicochemical properties. Although beta-HCH is not the main component of the technical HCHs, it has become the most abundant isomer in the environment because of its persistence. The dominant transfer processes between the adjacent compartments were deposition from air to soil, air diffusion through the air-water interface and runoff from soil to water. Sensitivity analysis showed that degradation rate in soil, parameters related to major sources, and thickness of soils had the strongest influence on the model result. Results of Monte Carlo simulation indicated the overall uncertainty of model predictions, and the coefficients of variation of the estimated concentrations of HCHs in all the compartments ranged from 0.5 to 5.8.     

黄河兰州段悬移质泥沙对氨氮的吸附特性

实验研究了黄河兰州段不同粒径的悬浮泥沙对氨氮的吸附行为,拟阐释黄河兰州段水质自净的机制。通过分析探讨了含沙量、氨氮初始浓度、泥沙粒径和化学成分对氨氮吸附过程的影响。结果表明,准二级动力学方程和Langmuir模型能够较好地描述黄河兰州段不同粒径泥沙的吸附动力学和等温吸附过程(R20.9);含沙量对泥沙吸附氨氮作用具有显著影响,且氨氮吸附量和平衡时间与含沙量呈明显负相关性;氨氮初始浓度与氨氮吸附量及平衡时间呈正相关性;同时,泥沙颗粒越细,吸附氨氮的能力越强,吸附容量越大,反应的自发程度越高。此外,泥沙有机质、Fe2O3、Al2O3和MgO的含量随粒径减小而增大,它们对单位质量泥沙最大吸附量(Sm)具有正效应。泥沙的吸附在黄河兰州段水质自净过程中起着一定的促进作用。     

陶粒生物滤池低温处理黄河水研究

进行了利用陶粒生物滤池工艺低温生物预处理黄河微污染水的研究,结果表明,温度的降低对陶粒生物滤池去除CODMn、UV254和氨氮的影响不明显,其平均去除率分别为11%、22.2%和61.2%。水温低于5℃时出水中亚硝酸氮浓度升高。此外,低水温条件下陶粒上生物膜脱氢酶活性仍然较高。     

Influence of diesel concentration on the fate of phenanthrene in soil

The aim of this study was to investigate the influence of diesel on the loss and bioavailability of soil-associated [14C]phenanthrene with time. In addition, the temporal development of phenanthrene catabolic activity and the impact of co-contaminant mixtures on the soil microflora were also assessed. With respect to compound fate, the results suggested that competitive effects between dissimilar co-contaminants did influence [14C]phenanthrene loss. Where diesel was present at a concentration of 0, 20, 200 and 2000 mg kg(-1), increased phenanthrene loss was observed with increasing diesel concentrations. In the 20,000 mg kg(-1) diesel treatment, however, a significantly higher amount of the initial [14C]activity remained after 225 days. Furthermore, initial degradation of phenanthrene in this treatment was retarded as a result of repressed phenanthrene catabolic activity. These results were complemented by a 4-fold increase in total culturable bacterial cell numbers in the 20,000 mg kg(-1) treatment when compared with the 2000 mg kg(-1) after 225 days of incubation time.     

Evaluation of aquatic environmental fate of 2,4,6-trichlorophenol with a mathematical model

A mathematical model, Simplified Approach for Fate Evaluation of Chemicals in Aquatic Systems (SAFECAS), was applied to evaluate fate of 2,4,6-trichlorophenol(TCP) in three types of aquatic environments; a river, an oligotrophic lake, and an eutrophic lake.Since phenols are dissociative substances, equilibrium constants and rate constants for transfer and transformation processes were measured or estimated as a function of pH.Results suggest that most of TCP is distributed to the water phase in aquatic environments, and is almost removed by the advective outflow in the river and by the photodegradation in lakes.     

黄河兰州段消落带表层沉积物对磷的吸附

为探究黄河消落带表层沉积物对磷的吸附特征,基于吸附动力学、吸附热力学及单因子实验,现场采集黄河 (兰州段) 消落带表层沉积物进行实验室模拟研究。结果表明：沉积物对磷的吸附动力学经历快速吸附、慢速吸附、吸附平衡3个阶段,扰动条件下,在10 min内吸附量达到最大吸附量的85%以上,480 min达到吸附平衡;沉积物对磷的吸附符合Langmuir吸附等温方程,随着温度的升高最大理论吸附量Q_m随之增加,25 ℃时Q_m达到119.831 mg·kg⁻¹;单因子实验中,扰动频率增加对磷的吸附量具有明显的促进作用;pH为7~8时沉积物吸附效果最佳,偏酸性条件次之,偏碱性条件下吸附效果较差;增大上覆水KH₂PO₄浓度,吸附量增加,吸附率整体呈下降趋势。由此可知,黄河消落带表层沉积物对磷元素具有一定的拦截效应,河水的扰动能够促进沉积物对PO₄^3--P的吸附,但是水体的pH值变化及高浓度陆源污染物均会削弱消落带对磷元素的吸附拦截作用。该研究结果可为黄河上游的水污染防治及消落带的生态管理提供研究依据。     

多环芳烃在淮河、黄河和卫河沉积物上的吸附及解吸行为研究

以淮河沉积物上多环芳烃的吸附研究为主线,以黄河、卫河沉积物为比对,研究菲和芘在3种河流沉积物上的吸附和解吸行为,重点考察吸附剂有机质组分、环境温度、吸附时间和共存物等因素对吸附的影响,找出可以用来预测这3条河流沉积物对多环芳烃吸附作用的模式。结果表明,菲和芘在3种河流沉积物上的吸附均呈非线性,可用Freundlich方程拟合,属放热反应、物理吸附。同一吸附质的有机碳归一化分配系数(Koc)数值相近,说明吸附剂有机质组分对吸附起主导作用;吸附能力随着吸附时间延长而增加,并与吸附质疏水性成正比;多环芳烃共存,有竞争吸附现象;辛醇/水分配系数可用来预测3种河流沉积物对多环芳烃的吸附作用;解吸存在滞后现象,吸附质疏水性强、吸附剂有机质含量高的体系,解吸滞后现象更加明显。     

Evaluating the environmental fate of atrazine in France

Atrazine is used in large quantities in U.S. and European countries as a weed-control agent. As a result, numerous data on its environmental fate and hazards have been published. Analysis of the literature shows that this herbicide can be found with appreciable concentrations in groundwaters, rivers, lakes, and estuaries. This contamination principally results from leaching and runoff processes. Atrazine can also pollute fog and rain due to its release into the atmosphere through spray applications. This large amount of information constitutes a very attractive basis for assessing the simulation performances of environmental fate models. In this context, CHEMFRANCE, a regional fugacity model level III which calculates the environmental distribution of organic chemicals in twelve defined regions of France has been used to estimate the environmental fate of atrazine. The calculated values are comparable with field and laboratory results. Therefore, CHEMFRANCE can be considered as a useful tool for simulating the environmental fate of this agrochemical.     

Evaluating the environmental fate of lindane in France

Lindane, a highly persistent and lipophilic pesticide, is still used in large quantities. This chemical can be found with appreciable concentrations in biota, atmosphere, and in other environmental compartments in the adsorbed form. This information provided a basis for assessing the simulation performances of CHEMFRANCE, a regional level III fugacity model allowing to generate environmental behavior profile of organic chemicals in France. The comparison between the estimated environmental fate and field and laboratory observations suggests that this fugacity model can be used to determine the processes that control the environmental fate of lindane in France. CHEMFRANCE also provides accurate estimates of environmental compartment contaminations.     

黄河兰州段、白银段重金属污染的磁学指标初探

对黄河兰州段、白银段的水样及沉积物样进行了环境磁学研究,并对部分样品进行了重金属含量分析.结果表明,污水的输入对河水的磁化率产生影响,且磁化率变化因污染源而异;亚铁磁性矿物主导了沉积物的磁性特征.重金属含量与磁参数的相关性均不显著,但在黄河白银段东大沟以下河段,重金属含量与非磁滞剩磁(ARM)、ARM/SIRM(SIRM为饱和等温剩磁)、频率磁化率(Xfd%)等磁参数有同步增强趋势,可能与细磁性晶粒对重金属的吸附作用有关.综合分析磁参数与重金属含量变化发现,河水Xfd%和ARM/SIRM可作为衡量部分重金属污染程度的参数.     

A multimedia environmental model of chemical distribution: fate, transport, and uncertainty analysis

This paper presented a framework for analysis of chemical concentration in the environment and evaluation of variance propagation within the model. This framework was illustrated through a case study of selected organic compounds of benzo[alpha]pyrene (BAP) and hexachlorobenzene (HCB) in the Great Lakes region. A multimedia environmental fate model was applied to perform stochastic simulations of chemical concentrations in various media. Both uncertainty in chemical properties and variability in hydrometeorological parameters were included in the Monte Carlo simulation, resulting in a distribution of concentrations in each medium. Parameters of compartmental dimensions, densities, emissions, and background concentrations were assumed to be constant in this study. The predicted concentrations in air, surface water and sediment were compared to reported data for validation purpose. Based on rank correlations, a sensitivity analysis was conducted to determine the influence of individual input parameters on the output variance for concentration in each environmental medium and for the basin-wide total mass inventory. Results of model validation indicated that the model predictions were in reasonable agreement with spatial distribution patterns, among the five lake basins, of reported data in the literature. For the chemical and environmental parameters given in this study, parameters associated to air-ground partitioning (such as moisture in surface soil, vapor pressure, and deposition velocity) and chemical distribution in soil solid (such as organic carbon partition coefficient and organic carbon content in root-zone soil) were targeted to reduce the uncertainty in basin-wide mass inventory. This results of sensitivity analysis in this study also indicated that the model sensitivity to an input parameter might be affected by the magnitudes of input parameters defined by the parameter settings in the simulation scenario. Therefore, uncertainty and sensitivity analyses for environmental fate models was suggested to be conducted after the model output was validated based on an appropriate input parameter settings.     

Assessment of the environmental fate of linear alkylbenzenesulphonates

Fugacity models, as developed previously, are applied to the chemical linear alkylbenzenesulphonate (LAS) to predict its ultimate fate in the environment. The behaviour of LAS is illustrated using unit worlds or evaluative environments at three successive levels of complexity (Levels I, II, and III). LAS is shown to have a short environmental life of two days attributable to rapid biodegradation in water. Reported concentration data for LAS in Rapid Creek, South Dakota, downstream from a municipal sewage treatment plant, are compared to expected concentrations as generated by the QWASI (Quantitative Water Air Sediment Interaction) fugacity model; the model being based solely on the physical, chemical, reactivity and transport properties of LAS and the emission rate of the chemical into the river. The data are found to fit the model when a sediment-water mass transfer coefficient of 7.80 × 10⁻³ m/h and an effective sediment bed depth of 3 mm are used. The generally satisfying agreement between environmental observations and the QWASI fugacity models lends credibility to the use of evaluative models.     

Effects of added PAHs and precipitated humic acid coatings on phenanthrene sorption to environmental Black carbon

Black carbon (BC; soot and charcoal) can be an extremely strong sorbent for organic compounds. In a previous study, sorption of d(10)-phenanthrene (d(10)-PHE) to BC in an unmodified contaminated sediment was found to be nine times less than that for BC isolated from this sediment. To find out the mechanism of this sorption attenuation (competition for BC sites between d(10)-PHE and native PAHs or blocking of BC sites by natural organic matter), we determined the effect on d(10)-PHE-BC sorption isotherms of additions of either PAHs or precipitated humic acid. Addition of humic acid did not significantly decrease BC sorption, whereas PAH additions (equal to the native PAH content in the original sediment) did, by about one order of magnitude. Therefore, competition between d(10)-PHE and the native PAHs could explain the whole attenuation of sorption to BC in unmodified sediments.     

Simulation of long-term environmental dynamics of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans using the dynamic multimedia environmental fate model and its implication to the time trend analysis of dioxins

Long term environmental fate of polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF) were studied using the fugacity-based dynamic multimedia environmental fate model. New formulation about soil wind erosion into air was included into the model. Effect of process assumption, sensitivity analysis for parameters, and tentative validation against the measured sediment core analysis was performed. Mass fluxes between compartments were estimated by the dynamic modeling. From the model estimates, major mass fluxes coming from emission source were shown to go to the soil and water through wet/dry deposition, then go to degradation mainly in the soil and sediment. Major mass fluxes of TCDD and OCDD come from the impurities in CNP (Chlornitrofen) and PCP (Pentachlorophenol) directly into the soil. Consideration about multimedia environmental dynamics using the modeled mass fluxes was shown in the discussion.     

Organophosphate and organophosphorothionate esters: Application of linear free energy relationships to estimate hydrolysis rate constants for use in environmental fate assessment

Hydrolysis rate constants required for assessing the environmental fate of certain organophosphate and organophosphorothionate esters may be estimated by use of linear free energy relationships (LFERs). LFERs for the second-order alkaline hydrolysis rate constants and the pKa of the conjugate acid of the leaving groups were established for 0,0-dimethyl- and 0,0-diethyl-0-substituted phosphates and phosphorothionates. Also, the second-order alkaline hydrolysis rate constants of selected triaryl phosphates were correlated with the Hammett-sigma constants. Existing LFERs for diaryl phosphate ester anions along with monoaryl phosphate ester mono- and dianions were used to predict hydrolytic half-lives under reaction conditions that are characteristic of aquatic environments.     

程序化的未确知测度模型用于水环境质量评价简

未确知测度模型用于水环境质量评价具有合理性。为使模型更加完善,提出将未确知测度模型建立过程标准化,使其具有通用性。并针对水质评价指标众多致评价过程复杂、计算量大的情况,利用MATLAB软件将标准化后的未确知测度模型设计为既定的程序,依靠计算机模拟来实现水质评价。通过对浮桥河水库水质的评价结果及与其他多种方法的对比,表现出标准化模型的客观性、合理性,MATLAB程序的实用性、快捷性。程序化的未确知测度模型标准化后可进行推广。