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1.
Metal pollutants in water poses great threats to living beings and hence requires to be monitored regularly to avoid loss of lives. Various analytical methods are available to monitor these pollutants in water and can be improved with time. Modelling of metal pollutants in any water system helps chemists, engineers and environmentalists to greatly understand the various chemical processes in such systems. Water samples were collected from waste water treatment plant and river from highlands close to its source all the way to the ocean as it passing through areas with high anthropogenic activities. Pre-concentration of pollutants in the samples was done through acid digestion and metal pollutants were analysed using inductively coupled plasma-optical emission spectra (ICP-OES) to determine the concentration levels. Metal concentrations ranged between 0.1356–0.4658 mg/L for Al; 0.0031–0.0050 mg/L for Co, 0.0019–0.0956 mg/L for Cr; 0.0028–0.3484 mg/L for Cu; 0.0489–0.3474 mg/L for Fe; 0.0033–0.0285 mg/L for Mn; 0.0056–0.0222 mg/L for Ni; 0.0265–0.4753 mg/L for Pb and 0.0052–0.5594 mg/L for Zn. Modelling work was performed using PHREEQC couple with Geochemist’s workbench (GWB) to determine speciation dynamics and bioavailability of these pollutants. Modelling thus adds value to analytical methods and hence a better complementary tool to laboratory-based experimental studies.  相似文献   

2.
In view of water pollutants becoming more complex, both anionic and cationic pollutants need to be removed. The multi‐pollutants simultaneous removal is paid more and more attention. Hence, development composite materials for treatment complex wastewater are the aim of this study. In this research, iron–nickel nanoparticles deposited onto aluminum oxide (α‐Al2O3) and carbon nanotubes (CNTs) to form nanocomposite materials Fe–Ni/Al2O3 and Fe–Ni/CNTs, respectively, were used as adsorbents. The adsorption capacities of Fe–Ni/Al2O3 and Fe–Ni/CNTs for AO7, HSeO, and Pb2+ were observed to be 5.46, 8.28, 27.02, and 25.6 mg/g, 15.29 and 17.12 mg/g, separately. The composite materials with negative charges were superior in adsorption of anionic pollutants. Using orthogonal experimental design and analysis of variance to co‐treat dye AO7, HSeO and Pb2+ in aqueous solutions, seven testing factors were included: (1) adsorbent types, (2) amount of iron, (3) solution pHs, (4) AO7 concentrations, (5) Pb2+ concentrations, (6) HSeO concentrations and (7) reaction time. The experimental results showed that the removal of complex pollutants AO7, HSeO, and Pb2+ on Fe–Ni/CNTs could reach up to 90% in the optimal treatment conditions. When using Fe–Ni/CNTs as the adsorbent, the sorption isothermals were well fitted in the Freundlich isotherm, and R2 could reach up to 0.98.  相似文献   

3.
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4.
Pyrite is a common sulfide mineral, particularly abundant in mining waste. It is a focus of mine envi-ronmental concern because the oxidation of exposed pyrite may lead to acid drainage and poisonous mate-rials (like As and heavy metals) release. In the United States, approximately $1000000 per day is spent in alleviating acid mine drainage[1], while the Canadian mining community has environmental liabilities that exceed $2 billion for disposal, management, and rec-lamation of mine waste[2]. …  相似文献   

5.
Determination of Atrazine, Terbutylazine and their Deethyl- and Hydroxymetabolites in Soil by SFE and HPLC/UV-DAD The supercritical fluid extraction (SFE) (CO2 and CH3OH as modifier) of the herbicides atrazine and terbutylazine as well as their deethyl- and hydroxymetabolites from soil was investigated. The analytes were determined after extraction by HPLC/UV-DAD using a C18 column. The limits of detection of the chromatographic step were between 0.01 μg/mL and 0.07 μg/mL, the relative standard deviations between 0.8% and 1.4%. With the aid of a control chart, the stability of the chromatographic system was evaluated. For extraction, soil was spiked with 5 μg/g for each component. For SFE, CO2 and methanol as modifier were used, and a pressure program was applied. Beside SFE, Soxhlet extraction with methanol and a solid-liquid extraction with acetone/water by shaking were carried out. For chlorine-containing triazines, the recovery rates were comparable for all extraction methods. The following recovery rates for SFE were obtained: deethylterbutylazine 77.4%, terbutylazine 80.2%, deethylatrazine 87.4%, atrazine 92.6%. However, the recovery rates for the hydroxymetabolites (4.1% for hydroxyatrazine, 21% for hydroxyterbutylazine) were not satisfying compared with the “classical” methods of extraction (above 50%). The limits of detection for the total process (SFE and HPLC/UV-DAD) estimated by the signal to noise ratio amounted 0.08 μg/g soil for chlorine-containing derivates, for hydroxyatrazine 2…3 μg/g, and for hydroxyterbutylazine 0.8 μ/g.  相似文献   

6.
The potential for humic substances to serve as a terminal electron acceptor in microbial respiration and to function as an electron shuttle between Fe(III)-reducing microorganisms and insoluble Fe(III) oxides was investigated. The Fe(III)-reducing microorganism Geobacter metallireducens conserved energy to support growth from electron transport to humics as evidenced by continued oxidation of acetate to carbon dioxide after as many as nine transfers in a medium with acetate as the electron donor and soil humic acids as the electron acceptor. Growth of G. metallireducens with poorly crystalline Fe(III) oxide as the electron acceptor was greatly stimulated by the addition of as little as 100 μM of the humics analog, anthraquinone-2,6-disulfonate. Other quinones investigated, including lawsone, menadione, and anthraquinone-2-sulfonate, also stimulated Fe(III) oxide reduction. A wide phylogenetic diversity of microorganisms capable of Fe(III) reduction were also able to transfer electrons to humics. Microorganisms which can not reduce Fe(III) could not reduce humics. Humics stimulated the reduction of structural Fe(III) in clay and the crystalline Fe(III) forms, goethite and hematite. These results demonstrate that electron shuttling between Fe(III)-reducing microorganisms and Fe(III) via humics not only accelerates the microbial reduction of poorly crystalline Fe(III) oxide, but also can facilitate the reduction of Fe(III) forms that are not typically reduced by microorganisms in the absence of humics. Addition of humic substances to enhance electron shuttling between Fe(III)-reducing microorganisms and Fe(III) oxides may be a useful strategy to stimulate the remediation of soils and sediments contaminated with organic or metal pollutants.  相似文献   

7.
In this study, ten best management practices (BMP) were implemented on agricultural areas in the Saginaw River Watershed using the Soil and Water Assessment Tool model based on four targeting methods (Load per Subbasin Area Index (LPSAI), Load per Unit Area Index (LPUAI), Concentration Impact Index (CII), and Load Impact Index (LII)). The effective BMPs both for targeting and non‐targeting pollutants were contour farming (CF) (except total nitrogen reduction during total phosphorus targeting scenario), residue management 1000 kg/ha and 2000 kg/ha, strip cropping, recharge structures, terracing, and native grass (NG). In contrast, conservation tillage and no tillage did not reduce significant amount of pollutants for any combination of targeting methods and priority areas. In regard to spatial correlation between targeting methods, a strong relationship was found between the LPSAI and LPUAI methods both for the sediment and total nitrogen targeting scenarios. In addition, a similar result was found between the CII and LPSAI targeting methods. Regarding the spatiotemporal variability of BMP implementation plan, distinct change in priority area was observed in the case of NG implementation by the end of the second year; however, this impact was minimal for CF due to less pollutant reduction efficiency compared to NG. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

8.
This study provides baseline information on the extent of contamination in sediments of the Jobos Bay estuary and surrounding areas in Puerto Rico. Sediments from Jobos Bay area (n = 14) had higher overall average concentrations than those from La Parguera area (n = 5, used as reference site), in μg/g dw, for As (17 vs 9), Cu (29 vs 14), Pb (11 vs 4), and Zn (64 vs 28); and in %, for Fe (2.6 vs 0.6). Sediments (n = 8) screened for PAHs and PCBs exhibited total concentrations (ng/g dw) that ranged from 40.4 to 1912, and from not detected to 11.21, respectively. The quality of sediments of Jobos Bay could be classified as low to moderate pollution. The proximity to anthropogenic sources of contamination warrants a monitoring program for inorganic and organic pollutants in Jobos Bay area for an effective coastal management program of this tropical ecosystem.  相似文献   

9.
Pi N  Tam NF  Wong MH 《Marine pollution bulletin》2011,63(5-12):402-411
Iron (Fe) plaque formed on mangrove root increased with wastewater discharge, but the extent was species-specific. For Bruguiera gymnorrhiza, Fe plaque concentration was 0.80 mg g(-1) root d.wt at Day 0 and increased to 4.59, 6.84 and 7.52 mg g(-1) at Day 75 in the fresh water control (FW), synthetic wastewater with pollutant concentrations five times of municipal sewage (5SW) and double of 5SW (10SW) treatments, respectively; the respective increases in Excoecaria agallocha were from 0.70 to 2.37, 10.73 and 13.21 mg g(-1). For Acanthus ilicifolius, similar increase was found in 5SW, but all of the plants were dead in 10SW at Day 75. The concentrations of heavy metals and phosphorus immobilized were positively correlated with the amounts of Fe plaque formed, but the regression coefficients varied among species. The performance of mangrove plants in wastewater treatments was related to the Fe plaque formed and its immobilized wastewater-borne pollutants.  相似文献   

10.
Annual variations in concentrations of Fe forms in the bottom water (0–70 cm from the bottom, by layers), pore water, and in solid phase of silts (25 cm, by layers) of the Krasnovidovo Pool channel area of the Mozhaisk Reservoir are studied. A drastic increase in the concentration and ratio of Fesusp/Fedis in the water layer 0–20 cm from the bottom is detected. Fe(II) dominates in dissolved and suspended forms. The concentrations of Fe(III) reaching 2–3 mg/l were for the fist time revealed in the pore water of silts (Eh ～ ?120 mV). The factors responsible for this phenomenon are discussed. Fe flux from sediments is tentatively assessed as 0.2–0.6 mg Fe m2/day.  相似文献   

11.
Suspended sediment adsorbs pollutants from flowing water in rivers and deposits onto the bed. However, the pollutants accumulated in the river bed sediment may affect the bio-community through food chain for a long period of time. To study the problem the concentration of heavy metals （Cr, Cd, Hg, Cu, Fe, Zn, Pb and As） in water, sediment, and fish/invertebrate were investigated in the middle and lower reaches of the Yangtze River during 2006-2007. The concentrations of heavy metals were 100-10,000 times higher in the sediment than in the water. Benthic invertebrates had relatively high concentrations of heavy metals in their tissues due to their proximity to contaminated sediments. Benthic invertivore fish had moderately high concentrations of heavy metals whereas phytoplanktivore fish, such as the silver carp, accumulated the lowest concentration of heavy metals. The concentrations of Cu, Zn, and Fe were higher than Hg, Pb, Cd, Cr, and As in the tissue samples. The concentration of heavy metals was lower in the river sediments than in the lake sediments. Conversely, the concentration of heavy metals was higher in river water than in lake water. While a pollution event into a water body is often transitory, the effects of the pollutants may be long-lived due to their tendency to be absorbed in the sediments and then released into the food chain. The heavy metals were concentrated in the following order： bottom material 〉 demersal fish and benthic fauna 〉 middle-lower layer fish 〉 upper-middle layer fish 〉 water.  相似文献   

12.
Thermoplastic resin pellets are melted and formed into an enormous number of inexpensive consumer goods, many of which are discarded after a relatively short period of use, dropped haphazardly onto watersheds and then make their way to the ocean where some get ingested by marine life. In 2003 and 2004 pre-production thermoplastic resin pellets and post-consumer plastic fragments were collected and analyzed for contamination for persistent organic pollutants (POPs). Samples were taken from the North Pacific Gyre, and selected sites in California, Hawaii, and from Guadalupe Island, Mexico. The total concentration of PCBs ranged from 27 to 980 ng/g; DDTs from 22 to 7100 ng/g and PAHs from 39 to 1200 ng/g, and aliphatic hydrocarbons from 1.1 to 8600 microg/g. Analytical methods were developed to extract, concentrate and identify POPs that may have accumulated on plastic fragments and plastic pellets. The results of this study confirm that plastic debris is a trap for POPs.  相似文献   

13.
In this study, the decolorization, dearomatization, and mineralization efficiencies of different advanced oxidation processes (AOPs; namely O3, O3/Fe(II), O3/Fe(II)/UVA, and O3/TiO2/UVA) were investigated for the azo dye C.I. Reactive Red 194 (RR194). The effects of pH (3–11), amount of TiO2 (0.05–1 g/L), and concentration of Fe(II) (0.1–1.6 mM) were investigated for the applied methods. The decolorization and mineralization efficiencies of the photocatalytic ozonation system (O3/TiO2/UVA) were increased by decreasing the pH of the dye solution in contrast to the ozonation system (O3). Decolorization of RR194 was increased in the photocatalytic ozonation system with an increasing amount of catalyst however, a decreasing was occurred for the homogeneous catalytic system (O3/Fe(II)) when increasing the concentration of catalyst. The decolorization efficiency of the homogeneous catalytic system (O3/Fe(II)) was enhanced when combined with UVA light. In our study, the most efficient method for dearomatization and mineralization was the O3/TiO2/UVA among the applied AOPs.  相似文献   

14.
Soret diffusion rise times were observed and resolved for Fe–Ni–S–P melts at 10 kbar in thermal gradients between 1300 and 1450°C. A steady-state separation of S-rich components to the hot end of the 2 mm long liquid charges is achieved in about 20 minutes. Chemical diffusivities of about 10−5 cm2/s are consistent with these observations and those of the compaction velocity of aggregates of crystalline Fe metal against the cold end of our experiments. These rapid diffusivities are not rapid enough for diffusion to be an important agent of bulk mass transfer in the addition or extraction of light elements in the Earth's core.  相似文献   

15.
High concentrations of air pollutants in the ambient environment can result in breathing problems with human communities. Effective assessment of health-impact risk from air pollution is important for supporting decisions of the related detection, prevention, and correction efforts. However, the quality of information available for environmental/health risk assessment is often not satisfactory enough to be presented as deterministic numbers. Stochastic method is one of the methods for tackling those uncertainties, by which uncertain information can be presented as probability distributions. However, if the uncertainties can not be presented as probabilities, they can then be handled through fuzzy membership functions. In this study, an integrated fuzzy-stochastic modeling (IFSM) approach is developed for assessing air pollution impacts towards asthma susceptibility. This development is based on Monte Carlo simulation for the fate of SO2 in the ambient environment, examination of SO2 concentrations based on the simulation results, quantification of evaluation criteria using fuzzy membership functions, and risk assessment based on the combined fuzzy-stochastic information. The IFSM entails (a) simulation for the fate of pollutants in ambient environment, with the consideration of source/medium uncertainties, (b) formulation of fuzzy air quality management criteria under uncertain human-exposure pathways, exposure dynamics, and SPG-response variations, and (c) integrated risk assessment under complexities of the combined fuzzy/stochastic inputs of contamination level and health effect (i.e., asthma susceptibility). The developed IFSM is applied to a study of regional air quality management. Reasonable results have been generated, which are useful for evaluating health risks from air pollution. They also provide support for regional environmental management and urban planning.  相似文献   

16.
Seventeen physical and chemical parameters were obtained from a hydroelectric reservoir located in a tropical region in the south of Brazil. Multivariate Principal Component Analysis (PCA) and Hierarchical Group Analysis (HGA) were used to identify the parameters discriminating the origin of water from the Tibagi and the Primeiro de Maio River, after it has passed the mixing region. The study was conducted during the dry and rainy seasons in July 2002 and February 2003 at three depths and three sampling sites located 0, 5, and 10 km away from the mixing region. The statistical methods showed to be appropriate for identifying the contribution of each tributary in the water mixing site of a complex water system. The most important discriminating parameter was the absorbance relation A(253 nm)/A(203 nm), followed by the concentrations of Fe(III), Mn(III), and Ni(II). An anthropogenic interference was found in the reservoir due to high Ni(II) and orthophosphate concentrations caused by a nearby town sewage discharge. The interference was more important during the dry periods due to the lower dispersion of the pollutants. Urgent initiatives should be taken from the state government to build treatment stations for the wastewater of the small cities around the Capivara hydroelectric reservoir to prevent the drinking water quality from deteriorating.  相似文献   

17.
Qualitative estimates of the relative iron and oxygen ions (Fe/O) in flows of solar cosmic rays from impulsive and long-duration solar flares are obtained for different ion energy ranges. The Fe/O value serves as a measuring unit for the known FIP effect in the solar atmosphere. It is shown that the FIP effect is most evident (maximum Fe/O values) in impulsive events for ions at energies <2 MeV/n. In long-duration events, the Fe/O value gradually decreases in parallel with ion energy and its maximum values are observable in the area of relatively low energies. The comparison of some flare models provided grounds for a qualitative explanation of the Fe/O behavior in response to changes in ion energies for both classes of solar cosmic ray (SCR) events.  相似文献   

18.
In order to assess pollutants and impact of environmental changes in the coastal region of the Jordanian Gulf of Aqaba, concentrations of six metals were traced through variations in 5 years growth bands sections of recent Porties coral skeleton. X-radiography showed annual growth band patterns extending back to the year 1925. Baseline metal concentrations in Porites corals were established using 35 years-long metal record from late Holocene coral (deposited in pristine environment) and coral from reef that is least exposed to pollution in the marine reserve in the Gulf of Aqaba. The skeleton samples of the collected corals were acid digested and analyzed for their Cd, Cu, Fe, Mn, Pb and Zn content using Flame Atomic Absorption Spectrophotometer (FAAS). All metal profiles (except Fe and Zn) recorded the same metal signature from recent coral (1925–2005) in which low steady baseline levels were displayed in growth bands older than 1965, similar to those obtained from fossil and unpolluted corals. Most metals showed dramatic increase (ranging from 17% to 300%) in growth band sections younger than 1965 suggesting an extensive contamination of the coastal area since the mid sixties. This date represents the beginning of a period that witnessed increasing coastal activities, constructions and urbanization. This has produced a significant reduction in coral skeletal extension rates. Results from this study strongly suggest that Porites corals have a high tendency to accumulate heavy metals in their skeletons and therefore can serve as proxy tools to monitor and record environmental pollution (bioindicators) in the Gulf of Aqaba.  相似文献   

19.
In oxic oceans, most of the dissolved iron (Fe) exists as complexes with siderophore-like, strongly coordinating organic ligands. Thus, the isotope composition of the little amount of free inorganic Fe that is available for precipitation and preservation in the geological record may largely be controlled by isotope fractionation between the free and complexed iron. We have determined the equilibrium Fe isotope fractionation induced by organic ligand activity in experiments with solutions having co-existing inorganic Fe(III) species and siderophore complexes, Fe-desferrioxamine B (at pH 2). The two differently complexed Fe(III) pools were separated by addition of Na2CO3, which led to immediate precipitation of the inorganic Fe without causing significant dissociation of Fe-desferrioxamine complexes. Experiments using enriched 57Fe tracer showed that isotopic equilibration between the 57Fe-labelled inorganic species and the isotopically “normal” siderophore-bound Fe was rapid during the first few seconds and then became slower. Consequently, the data fitted poorly to first and second order reaction equations. However, with a two-stage reaction, the data fit perfectly with a first order equation for the slower stage, indicating that approximately 40% re-equilibration may take place during the separation of the two pools. To further test if the induced precipitation leads to experimental artefacts, the fractionation during precipitation of inorganic Fe was determined. Assuming a Rayleigh-type fractionation during precipitation, this experiment yielded an isotope fractionation factor of 56Fesolution-solid = 1.00027. Calculations based on these results indicate that isotopic re-equilibration is unlikely to significantly affect our determined equilibrium Fe isotope fractionation between inorganically and organically complexed Fe. To determine the equilibrium Fe isotope fractionation between inorganically and organically bound Fe(III), experiments with variable proportions of inorganic Fe were carried out at 25 °C. Irrespective of the proportion of inorganic Fe, equilibrium fractionation factors were within experimental uncertainty, yielding an average fractionation factor, Δ56FeDFOB-inorg of 0.60 ± 0.15‰. The results indicate that equilibrium Fe isotope fractionation induced by strongly coordinating organic ligands may fractionate Fe isotopes in nature. The fractionation is likely to be important in oxic, Fe(III)-bearing environments, such as soils and rivers, and may, for example, largely control the Fe isotope composition of marine Fe–Mn crusts.  相似文献   

20.
This paper presents a critical review of model-input parameters for transport of on-site wastewater treatment system (OWS) pollutants. Approximately 25% of the U.S. population relies on soil-based OWS for effective treatment and protection of public health and environmental quality. Mathematical models are useful tools for understanding and predicting the transport and fate of wastewater pollutants and for addressing water-budget issues related to wastewater reclamation from site to watershed scales. However, input parameters for models that simulate fate and transport of OWS pollutants are not readily obtained. The purpose of this analysis is to illustrate an objective, statistically supported method for choosing model-input parameters related to nitrogen (N) and phosphorus (P). Data were gathered from existing studies reported in the literature. Cumulative frequency distributions (CFDs) are provided for OWS effluent concentrations of N and P, nitrification and denitrification rates, and linear sorption isotherm constants for P. When CFDs are not presented, ranges and median values are provided. Median values for model-input parameters are as follows: total N concentration (44 mg/L), nitrate-N (0.2 mg/L), ammonium (60 mg/L), phosphate-P (9 mg/L), organic N (14 mg/L), zero-order nitrification rate (264 mg/L/d), first-order nitrification (2.9/d), first-order dentrification (0.025/d), maximum soil capacity for P uptake (237 mg/kg), linear sorption isotherm constant for P (15.1 L/kg), and OWS effluent flow rates (260 L/person/d).  相似文献   

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