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The role of humic substances in chromium sorption onto natural organic matter (peat) 总被引:5,自引:0,他引:5
To elucidate mechanisms of Cr3+ sorption onto the unaltered solid natural organic matter, the comparative studies of this ion binding from a solution at pH 4.0 onto three selected particle size fractions: 2000–1000 μm, 630–200 μm and 63–20 μm of markedly different HS content and structure, separated by a wet sieving from an overall sample of peat (Brushwood Peat Humus) were carried out. Comparable patterns of COOH groups and CECt confirmed that for cation exchange capacity were responsible mainly cations connected with COO− functional groups. It was though found that aliphatic acids in the solid state did not take part in Cr3+ binding, thus the finest studied fraction 63–20 μm of the highest contents of functional groups showed the lowest sorption capacity for Cr3+, while similar patterns of sorbed Cr3+, soluble HS content and base CEC0 indicated that these parameters were directly interrelated. The base ion exchange processes determined by CEC0 (with Ca2+ as a predominant exchangeable cation) appeared to be not the major mechanisms responsible for Cr3+ sorption. For this metal, strong binding to insoluble large molecular weight organic pool two- to threefold prevailed over the ion exchange processes. Very low acid desorption indicated generally low mobility of Cr3+-organic compounds. 相似文献
64.
交流电场联合有机物料强化东南景天修复重金属镉污染土壤 总被引:1,自引:0,他引:1
针对土壤重金属污染植物修复效率低的问题,采用盆栽实验,通过施加多种强度的交流电场(0、0.5、1.0 V·cm−1)和不同种类的有机物料(黄腐酸钾、紫云英),研究了交流电场及其与有机物料联合对重金属超积累植物东南景天修复重金属镉污染土壤效率的作用。结果表明,交流电场促进了东南景天的生长和对重金属的吸收,以0.5 V·cm−1作用最佳,在电场处理组20 d后东南景天地上部Cd积累量比不施加电场的处理组提高了48.1%。交流电场和有机物料联用可以进一步提升东南景天对土壤镉的累积,施加黄腐酸钾处理组有利于土壤酸可提取态Cd的提高,比对照组提高了16.35%。在交流电场为0.5 V·cm−1条件下,以0.3%施用效果最佳,施加黄腐酸钾和紫云英分别是对照组(施加交流电场,不施加有机物料)的3.65倍和1.73倍。有机物料和交流电场的共同作用极大地促进了东南景天镉的积累。 相似文献
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Pesavento M Biesuz R Profumo A Soldi T 《Environmental science and pollution research international》2003,10(5):317-320
SCOPE: The detection and investigation of metal ions bound in strong complexes in natural waters is a difficult task, due to low concentration of the metal ions themselves, and also of the strong ligands, which, moreover, are often not of a well-defined composition. Here, a method is proposed for the investigation of the speciation of metal ions in natural waters. OBJECTIVE AND METHOD: It is based on the sorption of metal ions on strongly sorbing ion exchange resins, i.e. complexing resins. For this reason the method is called Resin Titration. It has been shown in previous investigations that the concentration of metal ion totally sorbed by a particular resin, and its reaction coefficient in the solution phase in the presence of the resin, can be determined from the sorption data using a simple relationship. Here, a data treatment (the Ruzic linearization method) is proposed for also determining the concentration of the ligands responsible for the complex in equilibrium with the resin. RESULTS: The method was applied to data obtained by Resin Titration of a freshwater and a seawater. Copper(II) and aluminium(III) were considered, using Chelex 100 as a titrant, due to its strong sorbing properties towards these metal ions. The results were: the total metal concentration in equilibrium with the resin, the side reaction coefficients, and the concentration of ligands. In all these cases the ligands forming very strong complexes were found to be at concentration lower than that of the metals. CONCLUSION: The Ruzic linearization method allows the determination of the concentration of the ligands forming very strong complexes in equilibrium with Chelex 100. The reaction coefficient was better determined by the calculation method previously proposed for RT. The ligands responsible for the strong complexes were found to be at low concentration, often lower than that of the metal ions considered. The metal in the original sample is partly bound to these ligands, since the complexes are very strong. Only a part of the metal is linked to weaker ligands, or free. 相似文献
66.
M. Fujii N. Shinohara A. Lim T. Otake K. Kumagai Y. Yanagisawa 《Atmospheric environment (Oxford, England : 1994)》2003,37(39-40):5495
Phthalate esters are used as plasticizer in many plastics, and several studies have shown their toxicity. Phthalate esters are gradually emitted over time, and so it is conceivable that they pose a significant health risk. This study aims to investigate the temperature dependence of the emissions of various phthalate esters and to estimate the health risks of these emissions at various temperatures. A passive-type sampler was developed to measure the flux of phthalate esters from the surface of plastic materials. With this sampler, we examined three widely used plastic materials: synthetic leather, wallpaper and vinyl flooring. The observed maximum emissions of diethyl phthalate, dibutyl phthalate, and diethylhexyl phthalate (DEHP) from these materials at 20°C were 0.89, 0.77, and 14 μg m−2 h−1, respectively. Emissions at 80°C were 2.8, 4.5×102, and 1.5×103 μg m−2 h−1, respectively. The results showed this temperature dependence is determined primarily by the type of phthalate ester and less so by the type of material. The estimation from the results of temperature dependence indicated the concentration of DEHP in a vehicle left out in the sunshine during the day can exceed the recommended levels of Japan Ministry of Health, Labour and Welfare. 相似文献
67.
垃圾渗滤液是一种高浓度难降解废水,含有大量有毒物质和溶解性有机质(dissolved organic matter, DOM),可生化性差。Fenton试剂(Fe2++H2O2)能产生活性极强的羟基自由基(·OH),能快速氧化渗滤液中DOM和微量有机物质。本研究采用Fenton法处理垃圾渗滤液,结果表明,在优化的处理条件下,渗滤液COD和TOC去除率分别为65%和42%,其中混凝作用去除的COD和TOC分别为20%和21%。进一步通过紫外可见光谱扫描、SUVA254、E3/E4等指标评价,发现Fenton法可以有效降低渗滤液中的DOM含量,大分子有机物的含量明显减少,而分子量小的有机物含量相对增加,反应体系中溶解性有机物分子量随着反应的进行而降低,腐殖化程度降低。利用GC-MS定性出渗滤液原液中47种有机物,该类有机物在Fenton反应后上清液中未再检出,但5种物质(邻苯二甲酸二(2-乙基己)酯、植酮、角鲨烯、麥角甾烷醇和二氢胆固醇)在沉淀的铁泥中检出。研究发现不同pH值、H2O2和Fe2+浓度条件下,残留的COD与DOM、TOC和UV254存在显著的相关关系(R2> 0.9)。本研究结果为改进垃圾渗滤液处理工艺和探索DOM在Fenton过程中的降解行为提供科学依据。 相似文献
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