双水相气浮浮选光度法测定污水中痕量土霉素

提出了一种亲水有机溶剂(乙醇、正丙醇、四氢呋喃等)气浮浮选(双水相气浮浮选)分离/富集光度法测定污水中痕量土霉素(OTC)的新型绿色高效分析方法。利用自制的浮选装置,选择四氢呋喃作溶剂,氯化钠作分相剂,氢氧化钠溶液调节酸度,将N(iⅡ)与OTC形成的疏水性缔合物浮选至有机相,浮选完毕后经分光光度法分析,线性范围为1.1×10-7～9.7×10-5mol/L,线性回归方程为A=2.038×105C(mol/L)+0.005,相关系数为0.9996,检出限为7.36×10-8mol/L,回收率为99.8%～100.4%,表观摩尔吸光率ε=2.038×105L/mol·cm,适用于污水中痕量土霉素的分离/富集及分析测定。     

Predicting the variation in detection function in line transect sampling through random parameter model

A method for calibrating (localizing) detection function models in line transect sampling is proposed. The method is based on a random parameter model which supplies localized predictions of detection function parameters utilizing a few sample data points from the concerned location(s). The method has the clear advantage of being able to provide density estimates based on very few observations from a location which would be impossible through traditional methods. The method is successfully illustrated using census data on sambar (Cervus unicolor) from a set of wildlife sanctuaries in Kerala, India. The need for further research in this direction is indicated.     

Calibration for the determination of 19 trace elements in serum and urine

A fast, high-throughput and accurate method was developed for determination of Al, As, Ba, Cd, Co, Cr, Cs, Cu, Fe, Mn, Ni, Pb, Se, U, Zn, Sb, Sn, I and Hg in urine and serum by inductively coupled plasma mass spectrometry. The samples were directly analyzed after 1/20 (v/v) dilution in 0.4% (v/v) HNO₃ and 0.005% Triton X-100. Three calibration modes were tested: aqueous and matrix matching with urine and serum. The accuracy was tested using reference materials of serum, urine and spiking. Results showed that the use of matrix matching calibration reduced the interferences and improved the recoveries for Al, Co, Pb and I in urine. The matrix matching did not affect the results considerably for serum. When serum was spiked with As, Co, Cs, Pb, U, Hg, I, Ba, Al, Cr and Ni, only matrix matching presented good recoveries. Helium was used as a collision cell gas reducing effectively polyatomic interferences for Al, Mn, Cu, Ni, Cr, Zn, As and Fe. Selection of the best internal standard was carried out for each element. The use of diluted HNO₃ improved the limit of detection. Finally, the method was applied successfully in samples of urine from workers occupationally exposed.     

三波段积分浑浊度仪的检测和校准

在兰州大学半干旱气候与环境观测站(SACOL)长期观测运行的基础上,针对测量气溶胶散射特性的三波段积分浑浊度仪(TSI3563)的校准和检测问题进行了探讨.讨论了TSI浊度仪检测和校准气体的选择,零气主要使用经高效微粒空气过滤器过滤的干净空气,标准气体主要使用CO2;总结出浊度仪零气检测和标准气体检测的理论依据,每天零气检测时,散射系数的变化范围为 ,平均值范围为 ,当超出这个范围就需要进行零点设定,每3~5d进行标准气体检测时,散射系数的平均值和理论计算值的误差超出 的范围,就需要进行全校准;最后介绍了零气校准和全校准的方法.     

Modeling agricultural non-point source pollution in a high-precipitation coastal area of China

Non-point source （NPS） pollution simulation in the high-precipitation coastal areas of China is difficult because varying annual typhoon incidence leads to highly contrasting rainfall patterns in dry years and wet years. An IMPULSE （Integrated Model of Non-point Sources Pollution Processes） based NPS model of the Changtan Reservoir watershed, which is a typical high-precipitation coastal area in China, was established based on the analysis of point and NPS pollution data, a digital elevation model, and data on land-use, soil, meteorology, economy, and agricultural management practice. Pre-processed pre-rain- fall soil moisture levels were introduced during the simulation to model the effects of typhoons on hydrology. Rainfall events were simulated sequentially through the year and the model was calibrated and verified using hydrological and water quality data. Accuracy of the simulated rainfall runoff and water quality in the Changtan watershed was found to be acceptable. The study showed that the NPS modeling system could be applied to the simulation and prediction ofNPS loadings in the Changtan Reservoir watershed.     

HYDROLOGIC MODELING AT THE WATERSHED SCALE USING NPSM1

ABSTRACT: The Nonpoint Source Model (NPSM) was chosen for nonpoint source pollutant modeling within three different watersheds. The first step in using NPSM, hydrologic calibration, is discussed here for three 8‐digit Hydrologic Unit Codes (HUCs) from the White River Basin in Indiana (Driftwood HUC), the Albemarle‐Pamlico River Basin in Virginia and North Carolina (Contentnea HUC), and the Apalachicola‐Chattahoochee‐Flint River Basin in Alabama, Georgia, and Florida (Ichawaynochaway HUC). Model predicted flows were compared statistically with USGS gauge data at the HUC outflow points for an uncalibrated and calibrated model run for the period from January 1, 1990, through December 31, 1992, and a validation run for the period from January 1, 1993, through December 31, 1995. Least squares regression of NPSM predicted flows versus USGS gauge data were 0.75, 0.44, and 0.69 for the calibration runs and 0.71, 0.69, and 0.64 for the validation runs in the Driftwood, Contentnea, and Ichawaynochaway HUCs, respectively. Nash Sutcliffe coefficient values were not as strong, ranging from ?0.66 to 0.45 for the calibration runs and 0.31 to 0.37 for the validation runs of the model. The Ichawaynochaway HUC proved the most difficult to calibrate indicating that the model may not be as useful in some geographic locations.     

PFC-APG-SA水成膜泡沫防治油液储运火灾实验研究

为有效防治油液在储运过程中易发生火灾问题,针对油液储运火灾特点,研发1种PFC-APG-SA水成膜泡沫材料。基于发泡性能、表面张力、pH值和抗烧性能,对复配的8种水成膜泡沫液开展性能测试实验,优选出最佳配方。结合分子动力学模拟,探究复配表面活性剂在模拟体系界面中分子排布作用的微观机理。研究结果表明：新型水成膜泡沫液发泡倍数为9.5,泡沫形态稳固,表面张力为17.521 mN/m,抗烧时间约为784 s,用量小且可以有效抑制油液燃烧;在分子动力学模拟中,复配的表面活性剂分子在油表面排列更为紧密,与油之间的相互作用能绝对值为8 210.238 kJ/mol,相互作用强且结构稳定。研究结果可为水成膜泡沫在油液储运火灾防治中的应用提供一定参考。     

单推三校正系数在光离子化检测器应用中的测量研究

在利用光离子化检测器监测单推三推进剂贮存环境时,必须首先要知道单推三相对于光离子化检测器校准气体的校正系数。通过简要介绍了校正系数的测量计算原理,并进行实验测量计算,求得单推三的校正系数。     

Partitioning of organochlorine pesticides from water to polyethylene passive samplers

The mass transfer rates and equilibrium partitioning behaviour of 14 diverse organochlorine pesticides (OCP) between water and polyethylene (PE) passive samplers, cut from custom made PE sheets and commercial polyethylene plastic bags, were quantified. Overall mass transfer coefficients, k_O, estimated PE membrane diffusion coefficients, D_PE, and PE-water partitioning coefficients, K_PE-water, are reported. In addition, the partitioning of three polycyclic aromatic hydrocarbons (PAHs) from water to PE is quantified and compared with literature values. K_PE-water values agreed mostly within a factor of two for both passive samplers and also with literature values for the reference PAHs. As PE is expected to exhibit similar sorption behaviour to long-chain alkanes, PE-water partitioning coefficients were compared to hexadecane-water partitioning coefficients estimated with the SPARC online calculator, COSMOtherm and a polyparameter linear free energy relationship based on the Abraham approach. The best correlation for all compounds tested was with COSMOtherm estimated hexadecane-water partitioning coefficients.     

Rates of particulate pollution deposition onto leaf surfaces: Temporal and inter-species magnetic analyses

Evaluation of health impacts arising from inhalation of pollutant particles <10 μm (PM₁₀) is an active research area. However, lack of exposure data at high spatial resolution impedes identification of causal associations between exposure and illness. Biomagnetic monitoring of PM₁₀ deposited on tree leaves may provide a means of obtaining exposure data at high spatial resolution. To calculate ambient PM₁₀ concentrations from leaf magnetic values, the relationship between the magnetic signal and total PM₁₀ mass must be quantified, and the exposure time (via magnetic deposition velocity (MV_d) calculations) known. Birches display higher MV_d (∼5 cm⁻¹) than lime trees (∼2 cm⁻¹). Leaf saturation remanence values reached ‘equilibrium’ with ambient PM₁₀ concentrations after ∼6 ‘dry’ days (<3 mm/day rainfall). Other co-located species displayed within-species consistency in MV_d; robust inter-calibration can thus be achieved, enabling magnetic PM₁₀ biomonitoring at unprecedented spatial resolution.