Chloride and atrazine transport through saturated soil columns

A possible contamination of water resources by the application of pesticides is a problem confronting many irrigated areas in arid and semi-arid areas. The best management practices have to be adopted to minimize pesticide transport and leaching under irrigated conditions. Atrazine dissipation in loam and sandy loam soils has been tested in the laboratory using disturbed soil columns under saturated flooding conditions. All the experiments were performed in replicates. The chloride transport was also studied to test its behavior as an inert tracer in both the soils. Atrazine and chloride breakthrough curves were analyzed with the parameter optimization program CXTFIT to determine transport parameters including pore-water velocity (v), retardation coefficient (R), hydrodynamic dispersion coefficient (D), and pulse duration (t _o ). The pore-water velocity and pulse duration of the solute were estimated from the experimental conditions and kept constant during the optimization procedure. The results indicated that the R of chloride was not significantly different from 1, indicating that chloride is an inert tracer for the types of soil tested in this study. The average R of atrazine was 4.56 and 3.15 for sandy loam and loam soils, respectively. Results also showed that the hydrodynamic dispersion coefficient was much higher in the case of sandy loam soil compared to the loam soil for the two solutes, thus indicating non-equilibrium transport conditions. In the case of chloride, D increased from 0.4 for the loam soil to 16.2?cm²/min for the sandy loam soil. Similar results were observed in the case of atrazine in which D for the sandy loam soil was 60% higher than that for the loam soil. More atrazine leaching is expected under field conditions due to the presence of soil cracks and macropores.     

离子选择电极法测定水中氯化物

采用离子选择电极法测定水中氯化物,通过试验确定参比溶液、离子强度调节剂的配制,并用添加氯离子氧化剂和离子浓度调节剂的方法排除干扰离子对测定的影响,使得复合氯离子电极测得的能斯特曲线响应系数为93．2％。标准品的加标回收率为99．8％±0．6％,测定结果的 RSD为0．4％。用该方法与国标硝酸银滴定法同时测定实际水样,两方法的测定值绝对误差在允许范围内。     

水体中总氮测定的影响因素及方法改进

对浊度、氯离子及高浓度氨氮对国标法测定总氮的影响进行分析。结果显示,浊度会使地表水中总氮测定的结果偏低,采用消解后3 500 r/min离心可以基本消除该影响;氯离子质量浓度3 000 mg/L时,对220 nm处吸光度值出现正干扰;水体中氨氮浓度较高时,会出现总氮测定结果严重偏低的现象,采用趁热摇匀法可以有效地避免高氨氮的干扰。     

Toxicity of road salt to Nova Scotia amphibians

The deposition of chemical pollutants into roadside wetlands from runoff is a current environmental concern. In northern latitudes, a major pollutant in runoff water is salt (NaCl), used as de-icing agents. In this study, 26 roadside ponds were surveyed for amphibian species richness and chloride concentration. Acute toxicity tests (LC₅₀) were performed on five locally common amphibian species using a range of environmentally significant NaCl concentrations. Field surveys indicated that spotted salamanders (Ambystoma maculatum) and wood frogs (Rana sylvatica) did not occupy high chloride ponds. American toads (Bufo americanus) showed no pond preference based on chloride concentration. Acute toxicity tests showed spotted salamanders and wood frogs were most sensitive to chloride, and American toads were the least. Spring peepers (Pseudacris crucifer) and green frogs (Rana clamitans) showed intermediate sensitivities. We concluded that chloride concentrations in ponds due to application of de-icing salts, influenced community structure by excluding salt intolerant species.     

Assessing the toxicity of sodium chloride to the glochidia of freshwater mussels: implications for salinization of surface waters

Chloride concentrations in surface waters have increased significantly, a rise attributed to road salt use. In Canada, this may be a concern for endangered freshwater mussels, many with ranges limited to southern Ontario, Canada’s most road-dense region. The acute toxicity of NaCl was determined for glochidia, the mussel’s larval stage. The 24 h EC50s of four (including two Canadian endangered) species ranged from 113-1430 mg Cl L⁻¹ (reconstituted water, 100 mg CaCO₃ L⁻¹). To determine how mussels would respond to a chloride pulse, natural river water (hardness 278-322 mg CaCO₃ L⁻¹) was augmented with salt. Lampsilis fasciola glochidia were significantly less sensitive to salt in natural water (EC50s 1265-1559 mg Cl L⁻¹) than in reconstituted water (EC50 285 mg L⁻¹). Chloride data from mussel habitats revealed chloride reaches levels acutely toxic to glochidia (1300 mg L⁻¹). The increased salinization of freshwater could negatively impact freshwater mussels, including numerous species at risk.     

Methyl chloride emissions from halophyte leaf litter: dependence on temperature and chloride content

Methyl chloride (CH₃Cl) is the most abundant natural chlorine containing compound in the atmosphere, and responsible for a significant fraction of stratospheric ozone destruction. Understanding the global CH₃Cl budget is therefore of great importance. However, the strength of the individual sources and sinks is still uncertain. Leaf litter is a potentially important source of methyl chloride, but factors controlling the emissions are unclear. This study investigated CH₃Cl emissions from leaf litter of twelve halophyte species. The emissions were not due to biological activity, and emission rates varied between halophyte species up to two orders of magnitude. For all species, the CH₃Cl emission rates increased with temperature following the Arrhenius relation. Activation energies were similar for all investigated plant species, indicating that even though emissions vary largely between plant species, their response to changing temperatures is similar. The chloride and methoxyl group contents of the leaf litter samples were determined, but those parameters were not significantly correlated to the CH₃Cl emission rate.     

Two-stage Sequential Electrochemical Treatment of Nitrate Brine Wastes

Nitrates in concentrated brines can be electrochemically reduced in the cathodic chamber of a split-cell electrochemical reactor with formation of ammonium (and small amounts of nitrite). Fortunately, ammonium may be electrochemically oxidized to nitrogen gas in the anodic reaction chamber if a coupled sequential process is used. The presence of chloride in the brine waste is an important consideration in oxidative electrochemical processes, however, because it cycles through oxidized and reduced states at the electrode surfaces and in the bulk solution. Electrochemical oxidation converts chloride ions to “active chlorine” species with additional oxidizing capability (chlorine, hypochlorous acid and hypochlorite – essentially bleach), as well as to chlorates, depending on the reaction conditions. The production of these active species improves treatment performance in the ammonium oxidation phase since oxidation is no longer limited to the electrode surface. However, the process must be engineered to minimize loss of process efficiency due to parasitic side reactions (chloramines and chlorate). In this study, two-stage batch electrolysis was conducted using a three-electrode (copper anode, platinum-coated titanium cathode, silver/silver chloride reference) electrochemical cell, with the anodic and cathodic chambers separated by a Nafion 117 membrane. Treatment of nitrate and ammonium was tested with and without the presence of chloride in the waste. No significant difference was observed in cathodic nitrate reduction with chloride present or absent. However, the presence of chloride in the solution favored overall soluble nitrogen elimination upon oxidation. Increasing applied current increased production of undesirable byproducts (especially chlorate).     

Testing the Hydrological Landscape Unit Classification System and Other Terrain Analysis Measures for Predicting Low-Flow Nitrate and Chloride in Watersheds

Elevated nitrate concentrations in streamwater are a major environmental management problem. While land use exerts a large control on stream nitrate, hydrology often plays an equally important role. To date, predictions of low-flow nitrate in ungauged watersheds have been poor because of the difficulty in describing the uniqueness of watershed hydrology over large areas. Clearly, hydrologic response varies depending on the states and stocks of water, flow pathways, and residence times. How to capture the dominant hydrological controls that combine with land use to define streamwater nitrate concentration is a major research challenge. This paper tests the new Hydrologic Landscape Regions (HLRs) watershed classification scheme of Wolock and others (Environmental Management 34:S71-S88, 2004) to address the question: Can HLRs be used as a way to predict low-flow nitrate? We also test a number of other indexes including inverse-distance weighting of land use and the well-known topographic index (TI) to address the question: How do other terrain and land use measures compare to HLR in terms of their ability to predict low-flow nitrate concentration? We test this for 76 watersheds in western Oregon using the U.S. Environmental Protection Agency’s Environmental Monitoring and Assessment Program and Regional Environmental Monitoring and Assessment Program data. We found that HLRs did not significantly improve nitrate predictions beyond the standard TI and land-use metrics. Using TI and inverse-distance weighting did not improve nitrate predictions; the best models were the percentage land use—elevation models. We did, however, see an improvement of chloride predictions using HLRs, TI, and inverse-distance weighting; adding HLRs and TI significantly improved model predictions and the best models used inverse-distance weighting and elevation. One interesting result of this study is elevation consistently predicted nitrate better than TI or the hydrologic classification scheme.     

Diffusion mechanism of chloride ions in sodium montmorillonite

For safety assessment of geological disposal of HLW, it is necessary to understand the diffusion mechanism of radionuclides in compacted bentonite. In this study, the diffusion behavior of chloride ions in compacted montmorillonite was studied from the viewpoints of the activation energy for apparent diffusion and the basal spacing of the compacted montmorillonite. A unique change in the activation energy as a function of the dry density of the montmorillonite was found. The activation energy decreased from 17.4 to 13.5 kJ mol-1 as the dry density increased from 0.7 to 1.0 Mg m-3 and increased to 25.1 kJ mol-1 at dry densities above 1.0 Mg m-3. The basal spacing of 1.88 nm, corresponding to the three-water layer hydrate state, was not observed by X-ray diffraction (XRD) until the dry density increased to 1.0 Mg m-3, where the minimum activation energy was obtained. On the other hand, a basal spacing of 1.56 nm, corresponding to the two-water layer hydrate state, was observed at the dry densities of 1.4 Mg m-3 and above, where the activation energies were more than 22 kJ mol-1. These experimental results suggest that there are at least two additional diffusion processes that can raise or reduce the activation energy and are affected by water in the region adjacent to the montmorillonite surfaces. If the "Grahame model" can be introduced to describe the electrical double layer, surface diffusion will be considered the possible predominant diffusion process, even for anions like chloride ions.     

城市垃圾焚烧中镉迁移转化及去除效率研究

通过典型城市垃圾焚烧炉烟气中镉排放浓度、镉排放速率、氯化氢排放浓度等进行现场监测,对比分析了不同氯化氢含量下,重金属元素镉向烟气中的挥发情况.对相关烟气监测参数分析发现,烟气中高温产生的氯化氢气体能够促进燃料中的重金属镉向烟气中的释放.烟气的排放速率影响重金属镉的去除效率,而烟气处理设施的类型对重金属镉影响不大.与单一的布袋除尘设施相比,布袋除尘器后加设活性炭喷射装置能够起到较好控制重金属镉排放的目的.