纳米氧化石墨烯对水中锶的吸附特征

采用纳米氧化石墨烯(GO)吸附放射性废水中Sr2+,从吸附原理、吸附动力学、pH对吸附的影响等方面对吸附过程进行研究.采用表面增强拉曼技术和红外光谱对Sr2+在GO表面的吸附进行光谱表征.将GO负载到活性炭表面进行柱实验探索GO在废水处理中的应用.结果表明,在pH值为6.0—6.5时GO对Sr2+的吸附符合Langmuir吸附模型,最大吸附量263.16mg·g-1.GO对Sr2+的吸附符合拟二级动力学方程.在pH3—11范围内吸附量随着pH升高显著增大.GO对Sr2+的吸附具有快速,吸附量大,适用pH范围广的特点,可大量用于放射性废水的处理.GO负载到活性炭上后吸附量有所下降,但克服了GO材料本身在水中粒径小难分离的缺陷,是一种可实际应用、去除环境中Sr2+的新方法.     

Use of SWAT to Estimate Spatial Scaling of Phosphorus Export Coefficients and Load Reductions Due to Agricultural BMPS

Phosphorus export coefficients (kg/ha/yr) from selected land covers, also called phosphorus yields, tend to get smaller as contributing areas get larger because some of the phosphorus mobilized on local fields gets trapped during transport to regional watershed outlets. Phosphorus traps include floodplains, wetlands, and lakes, which can then become impaired by eutrophication. The Sunrise River watershed in east central Minnesota, United States, has numerous lakes impaired by excess phosphorus. The Sunrise is tributary to the St. Croix River, whose much larger watershed is terminated by Lake St. Croix, also impaired by excess phosphorus. To support management of these impairments at both local and regional scales, a Soil and Water Assessment Tool (SWAT) model of the Sunrise watershed was constructed to estimate load reductions due to selected best management practices (BMPs) and to determine how phosphorus export coefficients scaled with contributing area. In this study, agricultural BMPs, including vegetated filter strips, grassed waterways, and reduction of soil‐phosphorus concentrations reduced phosphorus loads by 4‐20%, with similar percentage reductions at field and watershed spatial scales. Phosphorus export coefficients from cropland in rotation with corn, soybeans, and alfalfa decreased as a negative power function of contributing area, from an average of 2.12 kg/ha/yr at the upland field scale (~0.6 km²) to 0.63 kg/ha/yr at the major river basin scale (20,000 km²). Editor's note : This paper is part of the featured series on SWAT Applications for Emerging Hydrologic and Water Quality Challenges. See the February 2017 issue for the introduction and background to the series.     

密度泛函方法预测二英类化合物(PCDD/Fs)的正辛醇/水分配系数

在B3LYP/6-31G水平上全优化计算了多氯代二苯并一对-二(噁)英和多氯代二苯并呋喃(PCDD/Fs)系列物的分子结构;基于得到的分子结构描述符,依据修正的线性溶解能理论,分别建立了PCDDs和PCDFs的正辛醇/水分配系数的定量结构-性质关系模型(R2分别为0.985和0.966),并用交叉验证法对模型进行了验证(q2分别为0.983和0.936),用t-检验对各变量进行了检验.检验结果表明,模型的预测能力优于AM1法、单苯环氯取代指数法和拓扑量子方法得出的模型.     

Direct radiative forcing of urban aerosols over Pretoria (25.75°S, 28.28°E) using AERONET Sunphotometer data: First scientific results and environmental impact

The present study uses the data collected from Cimel Sunphotometer of Aerosol Robotic Network（AERONET） for the period from January to December, 2012 over an urban site,Pretoria（PTR; 25.75°S, 28.28°E, 1449 m above sea level）, South Africa. We found that monthly mean aerosol optical depth（AOD, τa） exhibits two maxima that occurred in summer（February） and winter（August） having values of 0.36 ± 0.19 and 0.25 ± 0.14,respectively, high-to-moderate values in spring and thereafter, decreases from autumn with a minima in early winter（June） 0.12 ± 0.07. The Angstrom exponents（α440–870） likewise,have its peak in summer（January） 1.70 ± 0.21 and lowest in early winter（June） 1.38 ± 0.26,while the columnar water vapor（CWV） followed AOD pattern with high values（summer） at the beginning of the year（February, 2.10 ± 0.37 cm） and low values（winter） in the middle of the year（July, 0.66 ± 0.21 cm）. The volume size distribution（VSD） in the fine-mode is higher in the summer and spring seasons, whereas in the coarse mode the VSD is higher in the winter and lower in the summer due to the hygroscopic growth of aerosol particles.The single scattering albedo（SSA） ranged from 0.85 to 0.96 at 440 nm over PTR for the entire study period. The averaged aerosol radiative forcing（ARF） computed using SBDART model at the top of the atmosphere（TOA） was- 8.78 ± 3.1 W/m2, while at the surface it was- 25.69 ± 8.1 W/m2 leading to an atmospheric forcing of ＋ 16.91 ± 6.8 W/m2, indicating significant heating of the atmosphere with a mean of 0.47 K/day.     

万宁地区近地面氯离子沉积速率的影响因素研究

目的 研究热带海洋大气环境中不同地貌下氯离子沉积速率的分布规律及主要影响因素。方法 通过挂片法采集万宁地区的氯离子沉积速率,并分析离海距离、地形地貌对氯离子沉积速率的影响,以及其与海水因素、自然环境因素间的相关性。结果 近海开阔区域氯离子沉积速率受离海距离和地貌的影响显著,在300 m处降低至90 m处的1/3左右,地貌的变化导致同一距离点处的氯离子沉积速率相差30倍。另外,高的海水有效波高、风速和东风占比使春季氯离子沉积速率高于夏季。结论 不同地貌下的氯离子沉积速率均与海水有效波高、风速间呈较强的正相关性。     

Aerosol scattering coefficients and major chemical compositions of fine particles observed at a rural site in the central Pearl River Delta, South China

During November-December 2010 aerosol scattering coefficients were monitored using a single-waved (525 nm) Nephelometer at a regional monitoring station in the central Pearl River Delta region and 24-hr fine particle (PM_2.5) samples were also collected during the period using quartz filters for the analysis of major chemical components including organic carbon (OC), elemental carbon (EC), sulfate, nitrate and ammonium. In average, these five components accounted for about 85% of PM_2.5 mass and contributed 42% (OC), 19% (SO₄^2-), 12% (NO₃^-), 8.4% (NH₄⁺) and 3.7% (EC), to PM_2.5 mass. A relatively higher mass scattering efficiency of 5.3 m²/g was obtained for fine particles based on the linear regression between scattering coefficients and PM_2.5 mass concentrations. Chemical extinction budget based on IMPROVE approach revealed that ammonium sulfate, particulate organic matter, ammonium nitrate and EC in average contributed about 32%, 28%, 20% and 6% to the light extinction coefficients, respectively.     

消防水幕衰减火灾辐射热的理论研究

从消防水幕系统中水滴粒子与火焰辐射热的散射和吸收作用出发,建立水滴与火焰辐射的数学模型;通过计算机求解获得了不同条件下水幕的隔热效率;并定量计算了水滴的粒径、荷载强度和水幕厚度对水幕透射率的影响;同时,计算并分析了目标体瞬态温度和平衡温度的变化规律。为了验证理论模型的可靠性,进行了全尺寸的火灾实体实验,理论预测和实验的结果比较接近。笔者的研究结果对于优化消防水幕设计和改进系统的性能在理论和实践上都具有一定的指导意义。     

Low to negligible photoactivity of lake-water matter in the size range from 0.1 to 5 μm

We found that the photochemical generation of reactive transients such as singlet oxygen and triplet states upon irradiation of different lake water samples is mostly accounted for by components smaller than 0.10 μm. Larger components often showed a much lower absorption and/or scattering of radiation compared with the smaller ones, with one exception where the minor to negligible photochemical activity of larger species was associated with significant radiation absorption/scattering. It is also shown that filtration of the lake water samples at 0.10 μm was able to effectively remove the suspended particles, differently from the usually suggested filtration at 0.45 μm.     

Investigation of partitioning mechanism for volatile organic compounds in a multiphase system

Laboratory experiments were performed to investigate the partitioning behavior of a set of diverse volatile organic compounds (VOCs). After equilibration at a temperature of 25 °C, the VOC concentrations were measured by headspace method in combination with gas chromatography/mass spectrometry (GC/MS). The obtained data were used to determine the partition coefficients (K_P) of VOCs in a gas-liguid-solid system. The results have shown that the presence and nature of solid materials in the working solution control the air-water partitioning of dissolved VOCs. The air/solution partitioning of BTEX and C₉-C₁₀ aldehydes was most affected in the presence of diesel soot. K_P values decreased by a factor ranging from 1.5 for toluene to 3.0 for ethylbenzene. The addition of mineral dust in the working solution exhibited greater influence on the partitioning of short aldehydes. K_P values decreased by a factor of 1.8. The experimental partition coefficients were used to develop a predictive model for partitioning of BTEX and n-aldehydes between air, water and solid phases.