首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 15 毫秒
1.
The sorption behavior of nonylphenol (NP, a toxic endocrine disruptor) on marine sediments was studied in detail through a series of kinetic and thermodynamic sorption experiments. The results showed that the sorption reaction of NP on marine sediments reached equilibrium in 1.5 h and that it accorded well with the non-linear Ho-McKay pseudo-second-order model. The sorption isotherms of NP on H2O-treated sediments could be well described by the Linear isotherm model, while the sorption isotherm on H2O2-treated sediments could be well fitted with the Freundlich isotherm model. A positive correlation was found between the distribution coefficient (Kd) and the sediment organic carbon contents. The medium salinity showed a positive relation with the Kd and a negative relation with the dissolved organic carbon (DOC). Hexadecyl trimethyl ammonium bromide (CTAB) enhanced the sorption amount of NP the most, while sodium dodecylbenzenesulfonate (SDBS) enhanced it the least. The sorption reaction of NP on marine sediments was a spontaneous, physical, exothermic and entropy-decreasing process.  相似文献   

2.
Yang Y  Liu M  Wang L  Fu J  Yan C  Zhou JL 《Marine pollution bulletin》2011,62(5):1025-1031
In the present study, phenanthrene was chosen as the probe compound for determining the sorption of PAHs in sediments from Yangtze estuary and nearby coastal area, China. Sorption isotherms were fitted well by the Freundlich and dual models, respectively. Selected sediments were further sequentially separated to remove the carbonate and organic carbon (OC). Calculated OC sorption capacity values based on both H2O2 oxidization and 375 °C combustion methods were similar and comparable to the Koc values estimated by the empirical linear sorption equations. Both sorption models and sorption data using sequentially separated samples achieve the similar conclusions: (1) the partition behavior dominated by OC in sediments with foc > 0.01; (2) for sediments with 0.001 < foc < 0.01, OC dominated sorption at relatively high aqueous concentration; whereas mineral phase adsorption dominated sorption at lower concentration especially when Cw/Sw was in the range of 0.0001-0.001 in natural aqueous system.  相似文献   

3.
A novel, simple method based on magnetic separation was developed for analytical purposes. In this method, N‐methyl‐D‐glucamine (NMDG) modified magnetic microparticles that were synthesized by using the sol‐gel method were used for the selective extraction and preconcentration of boron from aqueous solutions. This method combines the simplicity and selectivity of solvent extraction with the easy separation of magnetic microparticles from a solution with a magnet without any preliminary filtration step. The structure of the prepared γ‐Fe2O3‐SiO2‐NMDG (magnetic sorbent) composites were characterized by using X‐ray diffraction (XRD), Transmission Electron Microscopy (TEM), and Fourier Transform Infrared Spectroscopy (FTIR). The influence of different parameters on the sorbent capacity, such as the sorption/desorption of boron, magnetic sorbent dosage, pH, equilibrium time, type, and amount of stripping solution, were evaluated by using the magnetic sorbent. Any equilibrium pH greater than 6 can be used for sorption. Desorption from the sorbent was carried out by using 1.0 M HCl. The sorption and desorption efficiency of the γ‐Fe2O3‐SiO2‐NMDG was found as 92.5 ± 0.5% and 99.8 ± 6%, respectively.  相似文献   

4.
The paper describes the state of a standardized method for the determination of polycyclic aromatic hydrocarbons (PAH) in water, sludges, sediments, and soils by high performance liquid chromatography (HPLC). The separation of PAH on different specific PAH-columns is illustrated and the chromatographic conditions in relation to the subsequent programmed fluorescence detection are displayed. A method for the treatment of soil samples using a simple but efficient extraction method by ultrasonication using tetrahydrofuran or acetonitrile as extractants is presented. By means of selected samples, it is demonstrated that the extractive recovery rates of the presented method can compete with those of the conventional soxhlet extraction.  相似文献   

5.
The paper analyses the concentrations of total phosphorus and its forms in sediments from the Gulf of Gdańsk on the basis of studies conducted at 25 sampling sites in 2001–05. The phosphorus speciation analysis was performed by sequential extraction. The extensive spatial variability of Ptot concentrations and speciation was found to be dependent on the physicochemical properties of the sediments, the oxygen conditions in the water and sediments, and the depth of the water column above the sediment surface. In the coastal zone, the sedimentation of riverine suspended matter and the sorption and chemisorption processes exert a considerable influence on P speciation. Over 70% of variation of total phosphorus concentration in sediments in the Gulf of Gdańsk could be explained by changes of proportion of fine fraction of sediments (grain size <0.0625 mm). Maximum Ptot concentrations were recorded in clays and silts in the deep water, stratified part of the Gulf of Gdańsk. In the coastal zone, where sandy sediments are dominant, phosphorus concentrations were much lower; this was due to the considerable dynamics of the bottom water and intensive sea floor transport. Ptot concentrations in the Gulf of Gdańsk sediments ranged from 1.75 to 957.17 μmol g−1 d.w. Of all the forms of phosphorus, the highest concentrations were found for organic phosphorus (Org-P). Of its inorganic forms, the highest concentrations were of phosphorus bound to clay minerals and aluminium oxides (NaOH-P), the lowest ones were of loosely bound phosphorus (NaCl-P). On the basis of determinations of total phosphorus concentrations in sediments of a given type and the available data on the seabed areas covered by particular sediment types in the Gulf of Gdańsk, the mass of total phosphorus in the surficial sediment layer (0–2 cm) was estimated at ca. 15.6×103 tonnes.  相似文献   

6.
The aim of this study was to assess whether acoustic emission (AE) could carry information on preferential sorption/desorption of CH4 or CO2 in coal. AE and expansion/contraction of two nearly identical cylindrical coal samples were continuously monitored during displacement sorption experiments. One sample was subjected to presorption of CH4, followed by sorption of CH4/CO2 mixture. With the other one, presorption of CO2 preceded sorption of the mixture. The results obtained are the following: first, AE and stain kinetics show that the affinity of the coal tested is higher for CO2 than for CH4; second, methane is preferentially desorbed after presorption of CH4 — sorption of mixture of CH4 and CO2; third, during displacement sorption, kinetics of AE and sample swelling/shrinkage bring out the importance of presorption and the sorbate used. It matters whether the coal is first exposed to CH4 or to CO2. The present study has demonstrated that injection of CO2 into the coal previously exposed to CH4 causes considerable swelling of the coal. On desorption after CH4/CO2 exchange sorption, initial shrinkage is followed by swelling of the coal. These results could have implications for the sequestration of CO2 in coal seams and CH4 recovery from coalbeds (ECBM). Swelling/shrinkage of the coal matrix should be included in models used to predict coal permeability and gas flow rates. They also show that the AE technique can give more insights into coal matrix-gas interactions.  相似文献   

7.
《Marine pollution bulletin》2014,88(1-2):338-344
The concentrations of 22 polyaromatic hydrocarbons (PAH) in Posidonia oceanica seagrass, sediments, and seawater from the Alexandroupolis Gulf in the Aegean Sea, were investigated from 2007 to 2011. Temporal trends of total PAH contents in P. oceanica and sediments were similar. PAH levels in seawater, sediments, and seagrasses generally decreased with increasing distance from Alexandroupolis Port. Leaves and sheaths of P. oceanica had higher PAH levels than roots and rhizomes. P. oceanica accumulates PAHs and has good potential as a bioindicator of spatiotemporal pollution trends. PAH concentrations were also examined using in situ passive seawater sampling and were compared to results of passive sampling in the laboratory using local sediments and seawater. Levels of high molecular weight PAHs assessed using passive samplers confirmed the decreasing gradient of pollution away from Alexandroupolis Port. Passive sampling also proved useful for investigating sources of PAHs in P. oceanica meadows.  相似文献   

8.
The concentrations of 16 US EPA priority pollutant polycyclic aromatic hydrocarbons (PAHs) were analyzed in four size fractions (< 62, 62-125, 125-250, and > 250 microm) in three contaminated Boston Harbor sediments. Total PAH concentrations ranged from 7.3 to 358 microg/g dry wt. and varied largely among the different size fractions in these sediments. For all three sites, the highest PAH concentrations were associated with the large size (> 250 microm) fractions while the fine silt and clay fractions (< 62 microm) contained relatively low PAHs. Despite the great concentration differences, the composition of PAHs in the four size fractions of these sediments showed similar patterns dominated by PAHs with three or more rings. By examining the distribution patterns of selected alkyl homologs to parent compounds, the results indicate that the major PAHs contributing to the high contamination in the inner harbor sediments were from pyrogenic sources. A positive correlation between PAHs and sedimentary organic carbon exists for all size fractions in the sediments. Calculated organic carbon normalized partition coefficients (log K(oc)) for selected major PAHs indicate near-equilibrium partitioning of PAHs among the different size fractions despite their large concentration variations. Sedimentary organic matter associated with different size fractions was the controlling factor for the observed distribution differences of PAHs among the size fractions. Our results also suggest that sedimentary organic matter with different origins and maturities may have somewhat different PAH sorption characteristics. Particulate organic matter of charcoal, plant detritus and Capitella fecal pellets in the sediments appear to sorb PAHs more strongly than organic matter associated with clay minerals. The strong association of PAHs with these organic particles in sediments will have a great influence not only on their distribution but also on long-term environmental impact.  相似文献   

9.
有机质对城市污染河道沉积物铵态氮吸附-解吸的影响   总被引：2，自引：0，他引：2  
采集污染程度不同的城市河道沉积物(通吕运河、濠河和通甲河),在分析H2O2对沉积物有机质和铵态氮影响的基础上,分析沉积物在去除有机质前后铵态氮释放动力学和吸附热力学过程,研究城市污染河道沉积物有机质对铵态氮吸附-解吸的影响.结果表明:单位体积H2O2对有机质去除率随H2O2使用量增多而降低;去除有机质后,沉积物铵态氮含量显著增加,通吕运河、濠河和通甲河铵态氮最大含量分别是有机质去除前的4.16、3.55和2.85倍;沉积物对铵态氮的饱和吸附量随有机质含量减少而下降;沉积物铵态氮释放过程均表现为先快速释放,后减缓至平衡过程;去除有机质后,随着有机质含量的减少,沉积物铵态氮的最大释放量呈增大趋势;沉积物有机质和铵态氮含量是影响沉积物铵态氮释放的主要因素.  相似文献   

10.
Trace element study in Tisa River and Danube alluvial sediment in Serbia   总被引：2，自引：0，他引：2  
The contaminated sediment serves as a long-term source of toxic elements,since that mobility and transport in the environment of these elements are strongly influenced to associated solid phase.In this study,the modified Tessier sequential extraction procedure was applied for the fractionation of Cd,As,Hg,Cu,Zn,Cr,Pb,Ni and V in the sediments（Tisa River and canal sediments - Danube alluvial formation）,to obtain an overall classification of trace element pollution in these areas through its spatial distribution.Investigations of this region are important due to the widespread occurrence of metal mining activities throughout the Tisa and Danube drainage basins and possibilities of contamination with toxic elements at studies localities.Five steps of the sequential extraction procedure partitioned elements into CH3COONH4 extractable（F1）,NH2OH·HC carbonate extractable and easily reducible（F2）, H2C2O4/（NH4）2C2O4 moderately reducible（F3）,H2O2-HNO3 organic extractable（F4）,and HCl acid soluble residue （F5）.Analyses of the extracts were performed by flame atomic absorption spectrometry.To indicate the degree of risk of toxic elements,risk assessment code and contamination factor have been used.The results of partitioning study indicate that more easily mobilized forms（metals in adsorbed/exchangeable/carbonate forms or bound to amorphous Fe and Mn oxyhydroxides and Fe and Mn oxides） were predominant for copper,zinc,cadmium and lead,which can be used as indicators for input from anthropogenic source.In contrast,the largest amount of chromium and nickel were associated with the inert fraction,which reduced their solubility and rendered them immobile under natural conditions and indicative of natural origins.Most of remaining portion of metals was bound to ferromanganese oxides fraction.It is concluded that sequential extraction results proved useful to distinguish between anthropogenic and geochemical sources of elements in the sediments.  相似文献   

11.
This article describes laboratory batch sorption and column transport experiments that were conducted using heterogeneous alluvial sediments with a wide physical characteristic from wells, located between Lake Mogan and Lake Eymir, Gölbaşı, Ankara. The batch sorption experiment was conducted in two separate systems, that is, single and multicomponents. Single batch experiment was performed to determine equilibrium condition between the heavy metal ions and the soil adsorption sites. The sorption isotherms data from multibatch experiments were used to calculate the sorption parameters. Single batch experiment indicated that equilibrium was attained within 9 days from the start of the sorption test. As a result of multicomponents batch experiments, for Zn and Mn, the sorption process was well described by the Freundlich or Langmuir isotherm model, whereas sorption of Cu was better described by the linear isotherm model. The Kd of Cu were found to be highest in soil 1 (32550.350 L kg−1) and lowest in soil 5 (18170.76 L kg−1). The maximum and minimum sorption capacity values for Zn were found to be in soil 1 (10985.148 mg kg−1) and in soil 2 (8597.14 mg kg−1) units, respectively. [Correction added after online publication 15 July, 2010: In the preceding sentence, the words “minimum” and “maximum” were initially switched.] Similarly, soil 1 (7587.391 mg kg−1) and soil 5 (4908.695 mg kg−1) units provided the maximum and minimum values for Mn. In the column experiments, flow and tracer transport was studied under saturated conditions using conservative tracer to determine the transport parameters. Transport parameter values were obtained by curve-fitting using the nonlinear least-squares optimization code CXTFIT. Results of the column experiments indicated that the dispersivity values obtained for soil samples were in the range of 0.024 to 1.13 cm.  相似文献   

12.
无机盐改性对沸石覆盖技术控制底泥氮磷释放的影响研究   总被引：5，自引：0，他引：5  
通过试验,考察了无机盐改性对沸石覆盖控制底泥氮磷释放效果的影响,并对沸石覆盖技术控制底泥氮磷释放的机理进行初步探讨,结果表明:①NaCl及CaCl2改性对沸石吸附氨氮的性能影响不大;CaCl2改性可以提高沸石Ca2 的交换量而降低Na 的交换量,NaCl改性则可以明显降低Ca2 的交换量和增加Na 的交换量.②NaCl及CaCl2改性对沸石覆盖技术控制底泥氨氮的释放影响不大,而对控制底泥磷的释放则影响较大,沸石覆盖控制底泥磷释放效率从大到小依次为CaCl2改性沸石＞天然沸石＞NaCl改性沸石.③沸石覆盖技术控制底泥氨氮释放的机理为沸石的物理吸附和阳离子交换作用,控制底泥磷释放的机理包括沸石的机械阻挡作用和沸石与铵所交换出来的Ca2 对磷酸盐的固定作用.  相似文献   

13.
The fate of polycyclic aromatic hydrocarbon (PAH) contamination in a mangrove swamp (Yi O) in Hong Kong after an oil spill accident was investigated. The concentrations and profiles of PAHs in surface sediments collected from five quadrats (each of 10 m×10 m) covering different degrees of oil contamination and the most contaminated mangrove leaves were examined in December 2000 (30 days after the accident) and March 2001 (126 days later). The concentrations of total PAHs in surface sediments ranged from 138 to 2135 ng g−1, and PAHs concentrations decreased with time. In the most contaminated sediments, total PAHs dropped from 2135 (30 days) to 1196 ng g−1 (120 days), and the decrease was smaller in less contaminated sediments. The percentage reduction in sediment PAHs over three months (44%) was less significant than that in contaminated leaves (85%), indicating PAH in or on leaves disappeared more rapidly. The PAH profiles were very similar in sediments collected from quadrats Q1 and Q2 with benzo[a]anthracene and pyrene being the most abundant PAH compounds, but were different in the other three quadrats. The proportion of the light molecular weight PAHs to total PAHs increased after three months, especially phenanthrene. Results suggest that physical and photo-chemical weathering (tidal washing and photo-oxidation) of crude oil in surface sediments and on plant leaves were important processes in the first few months after the oil spill. The PAH contamination in Yi O swamp came from both petrogenic and pyrolytic sources. The petrogenic characteristic in the most contaminated sediment was confirmed with high values of phenanthrene to anthracene ratio (>10) and low values of fluoranthene to pyrene ratio (0.3–0.4).  相似文献   

14.
Lacustrine sediments were sampled from the inaccessible acidic (pH = 0.43) Nakadake crater lake of Aso Volcano, Japan by a simple method. The sediments contain an extremely high content (74 wt.%) of sulfur, which exits as elemental sulfur, gypsum and anhydrite. The abundant elemental sulfur is likely formed by the reaction of SO2 and H2S gases and by the SO2 disproportionation reaction in magmatic hydrothermal system below the crater lake. Based on the sulfur content of sediments and measurements of elevation change of the crater bottom, the sulfur accumulation rate at the Nakadake crater lake was calculated as 250 tonne/day, which is comparable with the SO2 emission rate (200–600 tonne/day) from the Nakadake crater. The sediments include a small amount (9%) of clear glass shards that are apparently not altered in spite of the high reactivity of hyperacid lake water. This finding suggests that the clear glass shards are fragments of recently emitted magmas from fumaroles on the bottom of the crater lake and the magma emissions continuously occur even in quiescent periods.  相似文献   

15.
Flow‐through column experiments were carried out to investigate the influence of pH on the sorption of three phenols (2‐methyl‐4, 6‐dinitrophenol, 2, 4, 6‐trichlorophenol, pentachlorophenol) onto a natural sandy aquifer material collected from a bank filtration site of River Elbe, Germany. For the phenols investigated, an increase in sorption (retardation) with decreasing pH is observed indicating a stronger sorption of the neutral species in comparison to that of the anions formed by dissociation. The anions of 2‐methyl‐4, 6‐dinitrophenol and 2, 4, 6‐trichlorophenol do not show significant sorption. On the contrary, pentachlorophenol showed sorption not only in neutral form but also in ionic form significantly which should be taken into account while assessing the fate and transport of such compound. A linear model based on the degree of protonation (calculated from pH and pKa) can be used to resolve the apparent (observed) sorption coefficient (Kd, app) into its neutral (Kd, n) and ionised (Kd, i) components. Knowing pKa, Kd, n, and Kd, i the apparent sorption coefficient for pH values other than experimentally investigated can be predicted.  相似文献   

16.
A field study was conducted in 2003 to estimate the areal distribution and concentrations of polycyclic aromatic hydrocarbons (PAH) in intertidal sediments at sites of past human and industrial activity (HA sites) in Prince William Sound (PWS), Alaska, the site of the 1989 Exxon Valdez oil spill. More than 50 HA sites, primarily in western PWS, were identified through analysis of historic records and prior field studies, and nine sites were selected for detailed surveys. The areal assessment process consisted of seven steps: (1) identify site from historic records and field surveys; (2) locate visual evidence of surface oil/tar at a site; (3) prepare a site map and lay out a sampling grid over the entire site with 10-m grid spacing; (4) excavate pits to 50 cm depth on the grid; (5) perform a field colorimetric test to estimate total PAH (TPAH) in sediments from the wall of each pit and record the results in the ranges <1 ppm; 1-10 ppm; >10 ppm TPAH; (6) expand grid size if necessary if elevated PAH levels are detected colorimetrically; (7) select 20 samples from each site for same-day shipboard PAH analysis by immunoassay (SDI RaPID PAH) and, based on these results, select sediment samples from each site for full PAH analysis in the laboratory to identify PAH sources. A total of 416 pits were dug at the nine sites. Nine acres of sediments with TPAH >2500 ppb dry wt. were mapped at the nine sites. TPAH concentrations obtained by immunochemical analysis of 181 samples from the nine sites ranged from 20 to 1,320,000 ppb (wet wt.). The contaminants are mixtures of petroleum products (2-3 ring PAH) and combustion products (4-6 ring PAH) unrelated to the 1989 Exxon Valdez oil spill. Mussels and clams collected at these sites have elevated levels of PAH that are compositionally similar to the PAH in the sediments. These findings indicate that at least a portion of the sediment PAH is bioavailable. The PAH sources at these historic industrial sites are chronic. They include relict fuel oil tanks and works located above and within the intertidal zone, with contamination at some locations extending into nearshore sub-tidal sediments. This study shows how a hierarchical approach can be used to quickly and successfully map, quantify, and subsequently, identify sources of PAH in shoreline sediments.  相似文献   

17.
Sediment transport related parameters in ephemeral streams may be used to model and delineate: (1) average dispersion patterns of copper-laden sediments; (2) differences in dispersion of copper in bedload and suspended sediments; and (3) variability in the copper-sediment dispersion patterns. A model that effectively describes dispersion of copper in ephemeral stream sediments in a simple mixing model: where Cr is the resultant concentration beneath the confluence of the main channel with a tributary, Ct is the concentration of metal in sediments of the tributary, Cm is the metal concentration in main channel sediments, and Xm and Xt are the basin areas or sediment yields of the main channel and tributary channel at their confluence. Variability in metal concentrations about values predicted by this model may be due to the different responses of bedload and suspended load to changes in stream hydraulics, the dynamics of bedload transport, the spatial and temporal variability rainfall within the drainage basin, and chemical mobility of the copper.  相似文献   

18.
Concentrations of the sum of 15 PAHs in 22 surficial sediment samples from the western Irish Sea ranged from below 100 ng g−1 in sandy sediments to a maximum of 1422 ng g−1 in the centre of the mud basin. The concentrations are typical of coastal shelf sediments, but greater than those observed for aquatic sediments remote from known anthropogenic sources. Organic C and the % sediment <15 μm were positively correlated with ΣPAH. ΣPAH was normalised to organic C and particle size (i.e. expressed as ΣPAH/Corg and ΣPAH/%<15 μm) and significant relationships were still observed with organic C and %<15 μm. The results are discussed in the context of using organic C to normalise concentrations of PAHs to assess contamination levels in sediments.  相似文献   

19.
古小治  姜维华 《湖泊科学》2018,30(6):1518-1524
借助微氧电极测试技术对太湖贡湖湾试验区疏浚后的新生界面溶解氧动态进行一年的跟踪调研,分析溶解氧在新生微米级界面的分布特征、扩散通量以及界面附近有机质矿化速率.结果表明疏浚后半年内,溶解氧在表层沉积物的侵蚀深度增大,氧化层明显加厚.氧气在新生界面表层沉积物中呈指数下降,但衰减相对较缓.在连续一年的跟踪调查中发现,仅秋季新生界面附近溶解氧浓度明显高于对照,而在其他月份无差异.污染底泥疏浚后一个月内氧扩散通量及有机碳矿化速率下降最为明显,仅为疏浚前的13%,其他月份沉积物-水界面氧的扩散通量、氧气的消耗速率、有机碳的降解速率均有不同程度下降,疏浚后新生界面氧气交换速率下降以及由此导致的有机碳矿化过程变缓可能深刻影响界面生源要素的迁移过程.  相似文献   

20.
The oxygen cycle and the balance of free oxygen and oxygen bound in CO2in Lake Baikal are discussed based on new data on the gas exchange between the lake and atmosphere, O2consumption in bottom sediments, and the rate of aerobic decomposition in the abyssal zone of the lake.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号