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1.
Determination of a Group Parameter for Organic Halogen Compounds in High Salt-laden Water Samples Using XAD-4 Resin Concerning the often discussed ‘chloride error’ in AOX determination, a method is described with allows the determination of the group parameter organic halogen compounds (OX) for chloride concentrations more than 1 g/L. In opposite to the standard method DIN 38409 part 14, no chloride influence up to a concentration of 10 g/L in real water samples occurs. The basis of the method is the adsorption of the organic compounds from the water sample on XAD-4 resin, a nonpolar copolymer of styrene and divinylbenzene. The organic compounds are concentrated on the XAD-4 resin conditioned with methanol. After the enrichment step, the adsorption columns are treated with sodium nitrate solution. Model experiments with p-chlorophenol and chloride concentrations of 50 g/L showed the effectiveness of this method. The loaded and washed adsorption columns are first eluated with acetone and then with ethyl acetate. Quantification of the OX compounds in the eluates is carried out by microcoulometric detection after combustion in a furnace equipped with a special injector for eluates. For optimal work, the instrument was modified and improved. The presented method was developed on model samples and tested on different real samples. 相似文献
2.
A method is described for the detection and identification of dissolved organic compounds (DOCs) in various water samples. Acid treated active silica gel sorbent (pH 3) was packed into a micro‐column and used as a solid‐phase extraction medium for adsorption of DOCs. Silica particles‐adsorbed‐organic species were then divided into equal portions followed by suspension into various organic solvents of different polarities such as methanol, acetone, ethyl acetate, and toluene. Suspended silica‐adsorbed‐organic species were shaken for 1 h at room temperature and the organic extracts were subjected to GC–MS analysis under temperature programming conditions for qualitative detection and identification of these species. Blank solvents and silica samples were also subjected to the same extraction procedures and GC–MS analysis for comparison. The mass spectrum of each eluted chromatographic peak was library searched or manually interpreted to identify the compound. 相似文献
3.
Christian Grøn 《Ground Water Monitoring & Remediation》1993,13(3):148-158
A regional survey of Danish ground water demonstrated the presence of adsorbable organic halogens (AOX) in almost all of 142 wells (99 percent). Generally, the presence of AOX was not related to point or non-point source contamination with halogenated organics. However, the AOX concentrations varied with the geology of the aquifers. Extractable organic halogens (EOX) and volatile organic halogens (VOX) were far less prevalent (detected in 4 percent of sampled wells) and the detection could, in most cases, be explained by contamination or chlorination of the wells. The VOX concentrations corresponded to the concentrations of identified, volatile contaminants. The study demonstrates the presence of a natural background level of AOX in the investigated aquifers. This must be considered in the interpretation of AOX results as an indicator of ground water contamination with haloorganics. Similar background levels of EOX or VOX were not delected. 相似文献
4.
Dissolved high molecular weight organic substances, like humic substances, can be characterized with regard to their molecular weight distribution using gel filtration chromatography (GFC). In addition, the adsorption properties, for example on activated carbon, can be described, if the substances are separated by hydrophobic interaction chromatography (HIC) in different fractions using a chromatographic column with a hydrophobic matrix. The retention time (Rt) of single chemical substances in this column can be used to characterize the hydrophobicity or hydrophility of each compound as well as of the high molecular weight organic matter. The hydrophobic interaction between the matrix of the column and the dissolved chemical compounds also depends on the hydrophobicity of the gel and the composition of the eluent. Relations between retention times, log P-coefficients (octanol/water partition) and K-values of isotherms on activated carbon (Freundlich equation) were found. 相似文献
5.
Gas-chromatographic Determination of Polychlorinated Biphenyls in Water after Headspace Solid-phase Microextraction Headspace-analytical techniques are usually applied to the determination of easily volatile substances in water, whereas semivolatiles are generally isolated by liquid-liquid or solid-phase extraction. In the present paper, a method is presented for isolating high boiling polychlorinated biphenyls (PCB) using headspace solid-phase microextraction at elevated temperature. In spite of their low vapor pressure, the analytes are adsorbed very efficiently on a poly-dimethylsiloxane-coated fiber. Thus, in combination with GC/ECD, a very simple and sensitive solventless determination of PCB is accomplished. Using the simplest possible standard conditions, limits of determination in the lowest nanogram-per-liter range are achieved. Further increased sensitivity down to the ppq (parts per quadrillion) range is possible by stirring and increasing the sample volume and adsorption time. Moderate matrix effects have been observed in some surface and groundwaters. 相似文献
6.
The diffusion and adsorption of two common volatile organic compounds, i. e., methanol and benzene, in different zeolite pellets were studied experimentally by using the single pellet moment technique. The experiments were conducted in a one‐sided single pellet adsorption cell at different temperatures in the range between 303 and 343 K. The results showed that both volatile organic tracers were adsorbed reversibly onto all zeolite samples. The overall adsorption equilibrium constants of both volatile organic compounds decreased with increasing temperature. The adsorption of the tracers onto the zeolite samples were found to increase in the order of NaY > clinoptilolite > 4A. In the range between 303 and 343 K, the adsorption constants of benzene range from 10.51 to 5.52 for zeolite 4A, from 11.90 to 6.37 for clinoptilolite and from 20.32 to 9.82 for NaY. The adsorption constants of methanol range from 19.05 to 8.26 for zeolite 4A, from 38.40 to 9.12 for clinoptilolite and from 74.21 to 14.70 for NaY at temperatures between 303 and 333 K. The effective diffusivities for benzene varied from 2.20·10–6 to 13.01·10–6 m2/s, whereas for methanol, they varied from 9.80·10–6 to 15.60·10–6 m2/s at the temperatures studied. 相似文献
7.
A manual SPME method is presented for the analysis of organic compounds in industrial wastewater. 24 compounds commonly found in the wastewater of a chemical plant in northern Germany have been selected as reference compounds. Precision, linearity, and detection limits have been determined. Moreover, the effect of methanol content, pH value, salt content, and an excess of compounds on the extraction process have been studied. Several compounds have been investigated for their applicability as internal standards to quantify the compounds of interest. Since the method will later be transferred to a fully automated SPME-GC system, which will be operated directly on-site at an industrial wastewater purification plant, special attention has been paid to the analysis of real wastewater samples. In this context, the fibre stability has been studied by performing 53 extraction/desorption cycles from one wastewater sample. Neither a decrease in fibre performance nor in precision has been observed indicating that the proposed method is suitable for the analysis of real wastewater. 相似文献
8.
This paper presents results of a study on the concentration of adsorbable organic halogens (AOX) in water samples of the Oder River and its tributaries collected from 1998 to 2002. The Vistula River water for AOX was analysed in the period 2001–2002. The investigated waters of the Vistula near the mouth (Kiezmark) were more contaminated with AOX than the Oder near the mouth (Widuchowa, Krajnik Dolny). In general, AOX levels in the Polish rivers are comparable to the values found in the European rivers, e.g. the Rhine and the Ton. The research has shown that AOX were correlated with pH, total suspended solids, and the riverine flow. No relation between dissolved oxygen and redox potential and AOX was found out. During the flood period AOX, inorganic halogens (TIX), and mineral substances (sulfates) were analysed. 相似文献
9.
Artefact-free Determination of Trihalomethanes in Chlorinated Swimming-pool Water Using Headspace Solid-phase Microextraction and Gas Chromatography Headspace solid-phase microextraction (headspace SPME) is a rather new technique for the solvent-free extraction and concentration of volatile substances from water into an organic polymer layer covering a fused-silica fiber. In combination with gas chromatography, the method represents a powerful tool for sensitive headspace investigations. As the adsorption of low boiling substances is favoured at low temperatures, the method can be operated at ambient temperature without formation of artefacts. Therefore, the method is ideally suited for the analysis of volatile disinfection by-products in water including several thermolabile THM-precursors. For the artefact-free determination of trihalomethanes it is superior to headspace gas chromatography under the conditions of the German standard method DIN 38407-F5. Compared to gas chromatography after pentane extraction (DIN 38407-F4), headspace SPME is simpler, less- laborious, better reproducible, and, especially for polar, easily water-soluble components, much more sensitive. In addition, it operates solvent-free and can be automated. Using a 100-μ polydimethylsiloxane-coated fiber, the method is linear over at least 2 orders of magnitude and has a relative standard deviation of 2… 7% in the upper ng/L range. With a 65-μ polydimethylsiloxane/divinylbenzene-coating on the fiber, the sensitivity of the method can be extended to limits of quantitation in the low ng/L range. However, this fiber, shows an increased susceptibility to matrix effects as observed in the presence of diisopentyl ether, which can only be compensated by using the method of standard addition. 相似文献
10.
Thermal methods are promising for remediating fractured geologic media contaminated with volatile organic compounds, and the success of this process depends on the coupled heat transfer, multiphase flow, and thermodynamics. This study analyzed field‐scale removal of trichloroethylene (TCE) and heat transfer behavior in boiling fractured geologic media using the multiple interacting continua method. This method can resolve local gradients in the matrix and is less computationally demanding than alternative methods like discrete fracture‐matrix models. A 2D axisymmetric model was used to simulate a single element of symmetry in a repeated pattern of extraction wells inside a large heated zone and evaluate effects of parameter sensitivity on contaminant recovery. The results showed that the removal of TCE increased with matrix permeability, and the removal rate was more sensitive to matrix permeability than any other parameter. Increasing fracture density promoted TCE removal, especially when the matrix permeability was low (e.g., <10?17 m2). A 3D model was used to simulate an entire treatment zone and the surrounding groundwater in fractured material, with the interaction between them being considered. Boiling was initiated in the center of the upper part of the heated region and expanded toward the boundaries. This boiling process resulted in a large increase in the TCE removal rate and spread of TCE to the vadose zone and the peripheries of the heated zone. The incorporation of extraction wells helped control the contaminant from migrating to far regions. After 22 d, more than 99.3% of TCE mass was recovered in the simulation. 相似文献
11.
MCPA (4‐chloro‐2‐methylphenoxyacetic acid) is an acidic herbicide widely used on olive crops in Spain. Due to its anionic form at natural soil pH, there is high risk of leaching and groundwater contamination by the use of this herbicide. The aim of this work was to study the effects of organoclay‐based formulations of MCPA and olive oil waste amendment on MCPA leaching in a sandy loam soil. For this purpose, batch adsorption and column leaching studies were performed. The organoclays used to prepare the clay‐based formulations of MCPA were obtained by treating Wyoming montmorillonite (SWy‐2) and Arizona montmorillonite (SAz‐1) with an amount of hexadecyltrimethylammonium (HDTMA) cation equal to 100% of the CEC of the montmorillonites. The organic residue used in this study was a solid waste from olive oil production (olive oil waste, OOW). The soil was amended with the organic residue at the rate of 10% (w/w). Batch release and column leaching studies indicated that organoclay‐based formulations of MCPA reduced the release rate and the leaching of the herbicide as compared to the use of a conventional formulation containing the herbicide in an immediately available form. The increase in soil organic matter of the soil upon amendment with the organic residue also resulted in greater adsorption and reduced leaching of MCPA in the soil. Accordingly, both the use of organoclay‐based formulations and the amendment of soil with OOW are proposed as efficient strategies to reduce extensive leaching losses associated with the application of MCPA in high‐risk scenarios, such as Mediterranean olive groves. 相似文献
12.
地球物理信号中普遍含有噪声，消除噪声是地球物理信号处理中的关键技术之一.奇异功率谱分析（SSA）是在状态空间（又称相空间）中研究（系统）动力学、非线性科学与混沌现象的方法.本文在状态空间中通过SSA分解，研究、应用地球物理序列的尺度不变性进行多维分形滤波：通过在状态空间的SSA分解，构造了经验正交函数系（EOF）；在EOF子空间中定义了两种尺度与测度后，发现了两种测度与尺度皆在多个尺度范围内存在尺度不变性；利用这种尺度~测度的尺度不变性，设计、实现了多维分形奇异功率谱(MSSA)滤波模型；处理解释了大洋钻探（ODP）1143A孔岩芯自然反射性（NGR）资料；Fourier功率谱分析结果证明，MSSA能有效地压制噪声，提取有用信号.研究得出，嵌入维数对MSSA基本无影响（小于1/1000），多维分形滤波器（MSSA）能有效压制噪声或提取有用信号. 相似文献
13.
Hydrophobic organic contaminants in marine water are mostly adsorbed onto (partitioned into) sediment organic matter (SOM). To study the impact of SOM diagenesis on sediment adsorption properties, artificial sediment with rich SOM content was incubated for more than 120 days. The sediment was sampled every week, and batch sediment adsorption tests were conducted with bisphenol A (BPA) and nonylphenol (NP) as the model pollutants. The results show that the amount of organic matter loaded in the sediment decreased by nearly 80% during incubation. For the incubated sediment, the BPA partition coefficient, Kd, decreased whereas the organic normalized partition coefficient, Koc, more than doubled. The experiments with NP show an even greater increase in Koc. Organic matter diagenesis shows a profound effect on the adsorption behavior of sediment, as the SOM residue has an increasing affinity and partition capacity for organic contaminants. 相似文献
14.
In this study, a generalized contaminant retardation factor applicable to a multiphase system where various types of colloids exist simultaneously with contaminants is derived and incorporated into an equilibrium model which is successfully applied to experimental data for which phenanthrene was used as hydrophobic organic contaminants and dissolved organic matter (DOM) or bacteria as mobile carriers. Based on the parameter values for the experimental data regarding the association of phenanthrene with solid matrix, DOM and various bacterial isolates, numerical experiments are performed to examine the transport behaviour of hydrophobic organic contaminants in various types of the multiphase system. Numerical experiments demonstrate that the extent of contaminant transport enhancement depends on the adsorption affinity of the colloid, its concentration and its mobility, and that the importance of a third phase to contaminant transport needs to be evaluated carefully with respect to the relevance of experimental conditions applied to realistic environmental conditions. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
15.
Accelerating the T‐matrix approach to seismic full‐waveform inversion by domain decomposition 
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下载免费PDF全文 A seismic variant of the distorted Born iterative inversion method, which is commonly used in electromagnetic and acoustic (medical) imaging, has been recently developed on the basis of the T‐matrix approach of multiple scattering theory. The distorted Born iterative method is consistent with the Gauss–Newton method, but its implementation is different, and there are potentially significant computational advantages of using the T‐matrix approach in this context. It has been shown that the computational cost associated with the updating of the background medium Green functions after each iteration can be reduced via the use of various linearisation or quasi‐linearisation techniques. However, these techniques for reducing the computational cost may not work well in the presence of strong contrasts. To deal with this, we have now developed a domain decomposition method, which allows one to decompose the seismic velocity model into an arbitrary number of heterogeneous domains that can be treated separately and in parallel. The new domain decomposition method is based on the concept of a scattering‐path matrix, which is well known in solid‐state physics. If the seismic model consists of different domains that are well separated (e.g., different reservoirs within a sedimentary basin), then the scattering‐path matrix formulation can be used to derive approximations that are sufficiently accurate but far more speedy and much less memory demanding because they ignore the interaction between different domains. However, we show here that one can also use the scattering‐path matrix formulation to calculate the overall T‐matrix for a large model exactly without any approximations at a computational cost that is significantly smaller than the cost associated with an exact formal matrix inversion solution. This is because we have derived exact analytical results for the special case of two interacting domains and combined them with Strassen's formulas for fast recursive matrix inversion. To illustrate the fact that we have accelerated the T‐matrix approach to full‐waveform inversion by domain decomposition, we perform a series of numerical experiments based on synthetic data associated with a complex salt model and a simpler two‐dimensional model that can be naturally decomposed into separate upper and lower domains. If the domain decomposition method is combined with an additional layer of multi‐scale regularisation (based on spatial smoothing of the sensitivity matrix and the data residual vector along the receiver line) beyond standard sequential frequency inversion, then one apparently can also obtain stable inversion results in the absence of ultra‐low frequencies and reduced computation times. 相似文献
16.
A highly sensitive and specific enzyme immunoassay (EIA) is described for the detection of the atrazine metabolite hydroxyatrazine. Polyclonal antibodies were raised in rabbits by immunization with a hapten-bovine serum albumin (BSA) conjugate containing 8 hapten residues per molecule of BSA. An EIA with a horseradish peroxidase (HRP) hapten tracer was optimized in microtitre plates. A concentration of 50% B/B0 was found at 0.10 μg/L for hydroxyatrazine. A limit of determination for hydroxyatrazine was reached at approximately 0.01 μg/L, i.e. well below the maximum concentration permitted by the EU guidelines for drinking water and the drinking water ordinance of the FRG. The assay did not require concentration or clean-up steps for drinking water or ground water samples. Validation experiments confirmed a good accuracy and precision. Hydroxyatrazine is reported to be the main atrazine metabolite found in soil samples. As organic solvents are usually employed for soil extraction, the influence of methanol as representative organic solvent on the assay was examined. Up to a concentration of 5% (v/v) methanol, the organic solvent did not affect the assay. 相似文献
17.
The influence of pH on the adsorption equilibria of a-picolin and phenol from aqueous solution on activated carbon is studied experimentally for the single solutes and their mixtures. For these weak bases and weak acids the effect of pH on adsorption capacity is contrary, thus allowing an efficient separation by adsorption. A model based on the concept of competitive adsorption of ionic and molecular forms of the organic electrolytes represents the experimental data qualitatively. Deviations between theoretical and experimental results are discussed on the basis of possible interactions of the organic solutes and the activated carbon with components of the buffer used in the experiments. 相似文献
18.
The pollution of underground and surface water streams is a tremendous environmental problem. Adsorption, in which activated carbon (AC) is used as an adsorbent, is one of efficient procedures to remove organic and inorganic pollutants from industrial wastewaters. Activated carbon fiber (ACF), a newly developed form of AC, has high adsorption rate and surface area and can be used for the treatment of industrial wastewaters. In this work, ACF was prepared by physicochemical activation method from kenaf and we studied its ability in the treatment of indigo‐containing wastewater produced from a dying factory. The filtered wastewater was treated via adsorption by ACF, and response surface experimental design method was used to study the effect of ACF dosage, contact time, temperature, and pH of the wastewater on the removal process. ACF dosage of 0.256 g, temperature of 12.5°C, pH 8.5, and contact time of 125 min were optimum treatment conditions. The adsorption process obeys pseudo‐second‐order kinetic and Freundlich isotherm models. 相似文献
19.
Factors Influencing the Release of DOC and AOX out of Former Wastewater Infiltration Soils The influence of soil and of infiltration water quality on the release of dissolved organic carbon (DOC) and adsorbable organic halogens (AOX) from two former wastewater infiltration sites was investigated in laboratory column studies. Desorption was the most important factor influencing release processes. It depends on the amount of sorbent and sorbate and the strength of binding. Therefore, for constant irrigation rates a higher soil organic carbon content coincided with higher DOC-contents of the column effluent, while the irrigation water quality was of minor importance. Within one system the dependencies of AOX release and DOC mobilization were found to be similar. Transferring these dependencies on other systems has its limitations because of a different binding quality between sorbent and sorbate. 相似文献
20.
为探究富营养化湖泊中自生源可溶有机质(DOM)在泥水界面的吸附行为,以马来眼子菜(Potamogeton malaianus)和铜绿微囊藻(Microcystis aeruginosa)释放的DOM为代表,考察针铁矿对草、藻源DOM中不同组分的吸附特征.三维荧光平行因子分析表明类富里酸组分C1和类胡敏酸组分C4的含量很低,而类蛋白物质(类酪氨酸组分C2和类色氨酸组分C3)分别占草、藻源DOM荧光组成的70%和93%. 2种DOM均可被针铁矿吸附,吸附过程符合伪一级动力学.通过等温线拟合发现针铁矿吸附藻源DOM的非线性更强,饱和吸附量(23.77 mg/g)高于草源DOM(19.10 mg/g).特别地,类蛋白组分呈现非线性吸附,而类腐殖物质的吸附近似线性,且针铁矿对于DOM各荧光组分的吸附量顺序为:C3C2 C4 C1,此非均质吸附特征与DOM组分的初始含量、分子大小、芳香性及有效吸附位点有关.红外光谱证实氨基、羧基和羟基是吸附过程中的重要官能团.因此,草、藻源DOM显著改变了针铁矿表面的有机物质组成,影响湖泊沉积物的生物地球化学行为. 相似文献