硒对水稻吸收积累和转运锰、铁、磷和硒的影响

采用土壤盆栽法研究硒对水稻吸收积累和转运锰、铁、磷和硒的影响.结果表明,土壤添加Se可导致水稻铁膜、根系、茎叶、谷壳和糙米中Se含量显著提高,水稻茎叶、谷壳和糙米中Mn含量显著降低.当土壤添加0.5 mg·kg-1Se和1.0mg·kg-1Se时,水稻茎叶Mn含量分别比对照处理降低32.2%和35.0%,谷壳Mn含量分别降低22.0%和42.6%,糙米Mn含量分别降低27.5%和28.5%.Se对水稻各部位的P和Fe(除谷壳外)含量影响不大.土壤添加Se对水稻铁膜、根系、茎叶和谷壳向糙米转运P和Fe的影响均不显著,但Se添加可以显著地降低水稻铁膜和根系向糙米中转运Mn的能力.与对照相比,土壤添加1.0 mg·kg-1Se导致Mn由铁膜和根系向糙米中的转运系数分别降低38.9%和37.9%.添加Se对水稻铁膜、根系、茎叶、谷壳和糙米中Mn、Fe、P和Se的分配比率也产生不同程度的影响.研究结果暗示可通过土壤添加Se来减少水稻对Mn的吸收积累和转运,从而降低Mn通过食物链途径对人体健康造成危害.     

Kinetic study of the gas-phase reaction of O3 with three unsaturated alcohols

Rate constants for the reactions of ozone with 1-octen-3-ol, 1-nonen-3-ol and 1-nonen-4-ol have been determined at 298 ± 1 K and atmospheric pressure for the first time. The experiments were performed in a 100-L FEP Teflon film bag using absolute rate method; the rate constants were(1.91 ± 0.19) × 10~(-17),(1.89 ± 0.20) × 10~(-17), and(0.83 ± 0.08) × 10~(-17)cm~3/(molecule·sec) for 1-octen-3-ol, 1-nonen-3-ol, and 1-nonen-4-ol, respectively. The rate constants have been compared with those of unsaturated alcohols structural homologs, and used to estimate the reaction reactivity. The electronegativity of carbon–carbon double bond was calculated by atomic charges analysis. The calculated results show that the electronic effect of the lone pair electrons of hydroxyl oxygen is the main cause of the difference in rate coefficient. According to the obtained rate constants, the atmospheric lifetimes of studied unsaturated alcohols were also estimated, which indicates that the reaction with ozone is an important loss pathway in the atmosphere, especially in polluted areas.     

环境监测技术竞赛方案设计

技术竞赛是促进监测水平提高的好方法,经过多次技术竞赛活动,制定出一套较科学适用的实施方案,基础理论采用笔试,样品测试采用尤登双样图。并设计出程序文件和测试样品配制方法,实际应用效果良好。     

沙渗滤去除三家店水库水中有机污染物的试验研究

采用CODMn和BOD作为指标对沙渗滤系统去除三家店水库水中有机污染物的效果进行了评价.试验构建一个长约10m、宽2m、高2m的砖混结构渗滤池,渗滤池分隔为8个小渗滤池,选择3种不同的沙分别构建1m3见方的渗滤床.渗滤系统持续运行125d,经历高温的夏季和低温的冬季,试验结果表明,渗滤系统对三家店水库水中有机污染物能有效去除,CODMn去除率一般在20%～40%,BOD的去除率一般在20%～80%,CODMn、BOD的出水值分别小于4mg·L-1、3mg·L-1;渗滤层厚度的增加不能显著增加有机污染物的去除率;温度对CODMn和BOD的去除有明显的影响;3种渗滤介质对CODMn和BOD均能有效去除,建筑沙对去除有机质的效果相对好一点.     

季节性缺氧水库铁、锰垂直分布规律及优化分层取水研究

经多年对阿哈水库Ｆｅ，Ｍｎ污染的研究表明，Ｆｅ，Ｍｎ分布随着季节为化、水库水温分层而变化，呈现明显的垂直分布规律，高浓度Ｆｅ、Ｍｎ主要出现在水温分层期水库中、下层、与库底缺氧、ＰＨ下降，沉积物中的Ｆｅ、Ｍｎ向上覆水释放造成的二次污染等密切相关，为自来水厂优化分层取水提供了依据。     

Operator-splitting errors in coupled reactive transport codes for transient variably saturated flow and contaminant transport in layered soil profiles

One possible way of integrating subsurface flow and transport processes with (bio)geochemical reactions is to couple by means of an operator-splitting approach two completely separate codes, one for variably-saturated flow and solute transport and one for equilibrium and kinetic biogeochemical reactions. This paper evaluates the accuracy of the operator-splitting approach for multicomponent systems for typical soil environmental problems involving transient atmospheric boundary conditions (precipitation, evapotranspiration) and layered soil profiles. The recently developed HP1 code was used to solve the coupled transport and chemical equations. For steady-state flow conditions, the accuracy was found to be mainly a function of the adopted spatial discretization and to a lesser extent of the temporal discretization. For transient flow situations, the accuracy depended in a complex manner on grid discretization, time stepping and the main flow conditions (infiltration versus evaporation). Whereas a finer grid size reduced the numerical errors during steady-state flow or the main infiltration periods, the errors sometimes slightly increased (generally less than 50%) when a finer grid size was used during periods with a high evapotranspiration demand (leading to high pressure head gradients near the soil surface). This indicates that operator-splitting errors are most significant during periods with high evaporative boundary conditions. The operator-splitting errors could be decreased by constraining the time step using the performance index (the product of the grid Peclet and Courant numbers) during infiltration, or the maximum time step during evapotranspiration. Several test problems were used to provide guidance for optimal spatial and temporal discretization.     

Spatial variability of arsenic and chromium in the soil water at a former wood preserving site

Contamination of industrial sites by wood preservatives such as chromated copper arsenate (CCA) may pose a serious threat to groundwater quality. The objective of this study was to characterise the spatial variability of As and Cr concentrations in the solid phase and in the soil water at a former wood impregnation plant and to reveal the fundamental transport processes. The soil was sampled down to a depth of 2m. The soil water was extracted in situ from the vadose zone over a period of 10 months at depths of 1 and 1.5m, using large horizontally installed suction tubes. Groundwater was sampled from a depth of 4.5m. Results showed that arsenic and chromium had accumulated in the upper region of the profile and exhibited a high spatial variability (As: 21-621 mg kg(-1); Cr: 74-2872 mg kg(-1)). Concentrations in the soil water were high (mean As 167 microg L(-1); Cr: 62 microg L(-1)) and also showed a distinct spatial variability, covering concentration ranges up to three orders of magnitude. The variability was caused by the severe water-repellency of the surface soil, induced by the concurrent application of creosote wood preservatives, which leads to strong preferential flow as evident from a dye experiment. In contrast to soil water concentrations, only low As concentrations (<12 microg L(-1)) were detected in the groundwater. High Cr concentrations in the groundwater (approx. 300 microg L(-1)), however, illustrated the pronounced mobility of chromium. Our study shows that at sites with a heterogeneous flow system in the vadose zone a disparity between flux-averaged and volume-averaged concentrations may occur, and sampling of soil water might not be adequate for assessing groundwater concentrations. In these cases long-term monitoring of the groundwater appears to be the best strategy for a groundwater risk assessment.     

高锰酸盐指数分析时加标回收率的测定

高锰酸盐指数分析一般不进行加标回收实验,因为加标回收率的实施对一个综合指标来说不易找到现成的标准物质,且容量法做加标回收存在一定困难,为加强高锰酸盐指数分析时准确度的控制,文章在加标回收率的测定方面做了积极的探索。     

Oxidation of Toluene on γ-Al2O3 Supported Copper–Manganese Catalysts

Abstract Catalytic incineration of toluene over γ-Al2O3-supported copper–manganese oxide catalysts in the temperature range of 433?K–553?K was investigated using a fixed-bed flow reactor. Catalysts were characterized using Brunauer-Emmett-Teller surface area analysis, scanning electron microscopy, temperature-programmed reduction, temperature-programmed oxidation, X-ray photoelectron spectroscopy, and X-ray diffraction. Incineration of toluene was achieved at temperatures up to 553?K and it was found that the weight ratio of reactants (Cu:Mn) was optimized to be 15:10. Brunauer-Emmett-Teller surface area results had no correlation with the activity of the catalysts. Results of temperature-programmed reduction/temperature-programmed oxidation and X-ray photoelectron spectroscopy showed that the redox peak of the 15Cu-10Mn catalyst shifted at lower temperatures and the binding energy shifted toward higher oxidation levels. These results show that high binding energy and high redox capacity are the causes of...     

火焰原子吸收光谱法测定苏州开发区26种蔬菜中铜锌铁锰镍

用火焰原子吸收光谱法测定了苏州开发区26种蔬菜中的铜、锌、铁、锰和镍的含量。蔬菜样品用硝酸高氯酸混合酸进行消解。4次测定值的相对标准差<5%,加标回收率在92%～107%之间。26种蔬菜中铜、锌、铁、锰、镍的含量基本均在世贸组织规定的范围内。