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The degradation pathway for the oxidation of EDTA in the UV/H2O2-process was investigated. In absence of iron ions, the mineralization of EDTA is dominated by the reaction of the HO-radicals generated by the photolysis of H2O2. The organic degradation products iminodiacetate (IMDA), glycinate, oxamate, glyoxylate, oxalate and formate, and the inorganic degradation products carbon dioxide, ammonia, nitrate, nitrite, and cyanate were found. In the presence of iron ions, photolytic decarboxylation processes inside the complex get an important role during degradation, and the organic degradation products ethylenediaminetriacetate (ED3A), ethylenediaminediacetate (EDDA), ethylenediaminemonoacetate (EDMA) were also found. By combining product studies with balances of carbon and nitrogen, the degradation pathway in the UV/H2O2-process could be elucidated. The degradation of EDTA was fast (kdeg = 0.012 s–1), and no toxic degradation products were identified. Therefore, the process is well suited for the elimination of EDTA in water treatment. 相似文献
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淋洗剂乙二胺四乙酸对重金属污染土工程特性的影响 总被引：1，自引：0，他引：1
以重金属铅（Pb2+）污染土和淋洗剂乙二胺四乙酸（EDTA）为研究对象,通过批次试验研究了不同浓度EDTA的淋洗对Pb2+污染土的渗透特性、持水特性、压缩特性、抗剪强度等工程特性的影响,为淋洗修复后土壤的二次利用提供参数支持。基于矿物成分、孔隙结构等微观试验,揭示了土壤工程特性变化的内在机制。研究结果表明,当淋洗剂EDTA浓度从0增加到0.15 mol/L,经淋洗修复后的污染土壤pH值从7.94下降到5.12,渗透系数降低超过一个数量级,黏聚力降低50%以上,而内摩擦角增大,持水性能提高,孔隙比从0.81下降到了0.76。微观试验的结果表明,随着淋洗剂浓度的增大,土壤中的蒙脱石、钠长石和伊利石矿物含量减少,石英矿物含量增加,其中蒙脱石含量从7.87%下降到了0.07%,而石英矿物含量增加了11.09%;淋洗后土壤单位质量进汞量由0.22 ml/g降低到0.15 ml/g,土壤总孔隙体积减少。重金属污染土淋洗修复工程在考虑重金属去除率及经济性指标的同时,还应考虑淋洗剂对土壤工程特性的弱化。 相似文献
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Barbara J. Cade-Menun Claudia R. Benitez-Nelson Perry Pellechia Adina Paytan 《Marine Chemistry》2005,97(3-4):293-306
Solution 31P nuclear magnetic resonance (NMR) spectroscopy has recently been used to characterize phosphorus species within marine particles. However, the effects of sample collection, storage and preparation have not been thoroughly examined. In this study, samples of settling particulates collected from a 1200-m sediment trap located in Monterey Bay, California, were subjected to various storage options (i.e., no storage, refrigeration, freezing, and oven-drying and grinding) prior to extraction for solution 31P-NMR spectroscopy. Freezing, refrigerating and drying samples for periods of up to 6 months prior to extraction with 0.25 M NaOH + 0.05 M Na2EDTA increased the concentration of extracted P by an average of 16% relative to samples extracted without storage. Pre-extraction storage also introduced some minor changes in P speciation, by increasing the percentage of orthophosphate by up to 15% and decreasing the percentage of pyrophosphate by up to 5%, relative to the abundances of these P species in samples extracted without storage. Drying caused the biggest changes in speciation, specifically decreasing more extensively the relative percentage of pyrophosphate compared to other treatments. Nevertheless, observed changes in speciation due to sample storage within a specific sample were small relative to differences observed among samples collected sequentially in the same area, or reported differences among samples collected at different locations. Samples were also analyzed by solid-state 31P-NMR spectroscopy before and after extraction, to examine extraction-related changes in P speciation. Comparison of solution with solid-state 31P NMR indicates that extraction with NaOH–EDTA removes the majority of organic esters, but only a variable portion of phosphonates (39–67%). In addition, there was preferential extraction of Ca-associated phosphate over Mg-, Fe- and Al-associated phosphate. Solution 31P NMR enables much higher resolution of P species within samples, particularly when it is important to speciate orthophosphate monoesters and diesters, or if polyphosphates are present. However, combining solid-state 31P NMR with solution 31P NMR spectroscopy for marine particles should be conducted when examining inorganic P speciation and the abundance of phosphonates. 相似文献
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Because of the influence of carbonates on the geotechnical properties of foundation and construction materials in civil engineering, a simple, precise, and inexpensive method of determining soil-carbonate content is needed. A large number of methods exist to determine the carbonate content in soils; but, for diverse reasons (precision (accuracy), cost, sensitivity, etc.) not all are appropriate in a civil-engineering laboratory. In the present work, different laboratory methods to determine the carbonate content in soils have been compared in order to choose the most appropriate one. The most suitable method has been selected on the basis of a number of general criteria: precision (accuracy), equipment cost, operating and maintenance costs, staff requirements, and sensitivity of the equipment. According to these general criteria, three methods can be considered suitable: flame photometry, volumetric calcimeter, and EDTA complexometry. These three methods present errors of less than 5%, involve low to medium cost, and the maintenance operations are simple. In addition, a suitability index has been defined (depending on three specific criteria: degree of precision (accuracy), level of standardization, and suitability of the operation method and type of ion analysed) which enabled the selection of the most appropriate from among the three methods. For the study, marl samples were taken from quarries used to construct the impermeable cores of three dams in the upper Guadalquivir River Basin (S Spain), as well as Standard samples were made with pure and inert calcium carbonate. Finally, it is concluded that the volumetric method (Bernard calcimeter) is the overall best technique to determine the carbonate content in civil-engineering laboratories. 相似文献
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The solubility of iron in oxic waters is so low that iron can be a limiting nutrient for phytoplankton growth in the open ocean. In order to mimic low iron concentrations in algal cultures, Ethylenediaminetetraacetate (EDTA) is commonly used. The presence of EDTA enables culture experiments to be performed at a low free metal concentration, while the total metal concentrations are high. Using EDTA provides for a more reproducible medium. In this study Fe speciation, as defined by EDTA in culture media, is compared with complexation by natural organic complexes in ocean water where Fe is thought to be limited. To grow oceanic species into iron limitation, a concentration of at least 10−4 M EDTA is necessary. Only then does the calculated [Fe3+] concentrations resemble those found in natural sea water, where the speciation is governed by natural dissolved organic ligands at nanomolar concentrations. Moreover, EDTA influences the redox speciation of iron, and thus frustrates research on the preferred source of Fe-uptake, Fe(III) or Fe(II), by algae. Nowadays, one can measure the extent of natural organic complexation in sea water, as well as the dissolved Fe(II) state, and can use ultra clean techniques in order to prevent contamination. Therefore, it is advisable to work with more natural conditions and not use EDTA to create iron limitation. This is especially important when the biological availability of the different chemical fractions of iron are the subject of research. Typically, many oceanic algae in the smallest size classes can still grow at very low ambient Fe and are not easily cultivated into limitation under ambient sea water conditions. However, the important class of large oceanic algae responsible for the major blooms and the large scale cycling of carbon, silicon and other elements, commonly has a high Fe requirement and can be grown into Fe limitation in ambient seawater. 相似文献
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The role of chloride ions in metal sulfides leaching has been well established by researchers, the complexation of chloride ions was considered to be the main effect of chloride ions. In this work, the complexation of chloride ions was neglected by addition of EDTA, a strong complexing agent. In this way, further study was conducted on the effect of chloride ions. The increase of chloride ions concentration from 0 to 2 mol/L, decreased the open circuit potential of pyrite from 264 to 91 mV. Unless otherwise stated, all potentials in this paper are based on the potential of saturated calomel electrode. At 600 mV, the increase of chloride ions concentration acceleraed pyrite oxidation; at 800 and 1000 mV, however, the increase of chloride ions concentration lowered pyrite oxidation rate, and the proportion of elemental sulfur was also decreased with increasing chloride ions concentration; when chloride ions concentration increased from 0 to 2 mol/L, the proportion of elemental sulfur decreased from 32% to 28.4% at 800 mV, and 7.1% to 2.4% at 1000 inV. 相似文献
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经典测定钙、镁含量的方法是用EDTA标准溶液滴定钙镁总量后再滴定钙,此方法对于含钙、镁离子盐水体系溶解度的测定,尤其在镁含量较高的情况下,其分析精度和准确度远远迭不到要求。针对硝酸钙、硝酸镁混合样品,采用EDTA质量滴定法测定钙镁总量,用草酸钙沉淀法从镁中定量分离钙,然后运用羔减法计算出镁的含量。实验结果表明,当混合溶液中镁钙的质量比不超过10：1时,钙、镁离子分析结果的相对误差在±0．3％之内,但镁钙的质量比超过10：1时,相对误差达到1％。因此,在一定的镁钙质量比范围内,此方法可用于盐水体系中钙、镁含量的准确测定。 相似文献
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EDTA络合滴定法是应用范围比较广的传统方法,但该方法对样品中钙镁摩尔比的适用范围约为1：10-10：1,时于超过该范围的钙镁比样品测定的准确度会有所下降;传统EDTA络合指示剂滴定法测定高钙低镁体系中钙镁含量时,终点不易判断,测定结果平行性差,甚至出现钙镁总量小于钙量的情况。通过往样品中加入一定量Mg’标准溶液的方法,改善了滴定反应效果。结果表明,Mg^2＋的加入能明显提高滴定终点变色灵敏度。加标回收试验表明,镁的回收率达到99．96％,钙的回收率达到99．40％。该方法准确度高,操作简单,适用性强。 相似文献