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1.
The To Lich and Kim Nguu Rivers, laden with untreated waste from industrial sources, serve as sources of water for irrigating vegetable farms. The purposes of this study were to identify the impact of wastewater irrigation on the level of heavy metals in the soils and vegetables and to predict their potential mobility and bioavailability. Soil samples were collected from different distances from the canal. The average concentrations of the heavy metals in the soil were in the order zinc (Zn; 204 mg kg?1) > copper (Cu; 196 mg kg?1) > chromium (Cr; 175 mg kg?1) > lead (Pb; 131 mg kg?1) > nickel (Ni; 60 mg kg?1) > cadmium (Cd; 4 mg kg?1). The concentrations of all heavy metals in the study site were much greater than the background level in that area and exceeded the permissible levels of the Vietnamese standards for Cd, Cu, and Pb. The concentrations of Zn, Ni, and Pb in the surface soil decreased with distance from the canal. The results of selective sequential extraction indicated that dominant fractions were oxide, organic, and residual for Ni, Pb, and Zn; organic and oxide for Cr; oxide for Cd; and organic for Cu. Leaching tests for water and acid indicated that the ratio of leached metal concentration to total metal concentration in the soil decreased in the order of Cd > Ni > Cr > Pb > Cu > Zn and in the order of Cd > Ni > Cr > Zn > Cu > Pb for the ethylenediaminetetraaceitc acid (EDTA) treatment. The EDTA treatment gave greater leachability than other treatments for most metal types. By leaching with water and acid, all heavy metals were fully released from the exchangeable fraction, and some heavy metals were fully released from carbonate and oxide fractions. The concentrations of Cd, Cr, Cu, Ni, Pb, and Zn in the vegetables exceeded the Vietnamese standards. The transfer coefficients for the metals were in the order of Zn > Ni > Cu > Cd = Cr > Pb.  相似文献   

2.
Estuarine systems adjacent to urban areas are at risk of contamination by contaminants from anthropogenic sources, such as heavy metals. We anticipated that the sediments of the Swan River estuary, which runs through metropolitan Perth in Western Australia, would show metal contamination related to industrialization and inputs of stormwater. Total Cu, Pb and Cd concentrations, and Cu, Pb, Cr and Zn inoperationally-defined fractions, were determined inseparate sampling exercises in near-shore sediments ofthe upper Swan River estuary.Total metal concentrations in sediments were not high (maximum values of 297 mg kg-1 for Cu, 184 mg kg-1 for Pb and 0.9 mg kg-1 for Cd) when compared with Australian environmental assessmentguidelines for soils. On the basis of linear regressions between sediment metal concentrations andphysicochemical properties of the sediments (pH, organic carbon, particle size distribution), no single parameter could explain the variation in metal concentrations for all metals. Sediment organic carbon content was positively correlated with Cu concentration; Cu concentrations also increased significantly with increasing clay content anddecreasing sand content. Pb concentrations showed a significant increase with increasing sediment pH, and were approximately three-fold higher in sediments adjacent to stormwater drain outfalls than in sediments remote from drains; no such effect was observed for Cu or Cd. No effect of distance downstream was observed. Sequential extraction of sediments showed that most of the metals were in relatively immobile forms, for example bound to Feoxides, or only extractable by aqua regia. The enhanced concentrations of Pb near stormwater outfalls suggest that vehicle-derived Pb may be an important contributor of Pb to the estuary.  相似文献   

3.
中国原油污染区重金属空间分布模式及其潜在来源研究   总被引：1，自引：0，他引：1  
Twenty-two soil samples were collected at the subregional scale （50 km2） around Gudao Town, a typical oil-producing region of the Shengli Oilfield in the Yellow River Delta, China to determine the spatial distribution patterns and potential sources of heavy metals in soils of crude oil-polluted regions. The concentrations of total petroleum hydrocaxbons （TPHs） and heavy metals as well as other soil properties were determined and the enrichment factor values were calculated for the heavy metals measured. Principal component analysis （PCA） and cluster analysis （CA） were used to estimate potential sources contributing to the concentrations of heavy metals in the soils. The results revealed that the soils were slightly alkaline （pH = 7.33-8.05） and high in salinity （1.43-41.30 g kg-1）, TPHs （0.51 28.40 g kg-1） and organic matter （1.74-31.50 g kg-1）. The mean concentrations of the measured heavy metals Cu, Zn, Pb, Cd, Cr, Ni and V were 18.4, 78.2, 20.8, 0.19, 56.6, 26.3 and 62.1 mg kg-1, respectively. Although the concentrations of all the metals measured in this study were not high enough to exceed the national control standards, there was a significant enrichment of Cd in the study area and Zn and Ni were in the category of deficiency to minimal enrichment. The spatial distribution patterns of Cu, Cr, Ni and V were similar and partially affected by oil exploitation and petroleum hydrocarbon spills. Potential sources of Cr, Ni, V and Cu in the soils were both natural sources and petroleum hydrocarbon spills, while Zn, Pb and Cd were probably from anthropogenic sources such as farming activities and traffic.  相似文献   

4.
The bioavailability and plant uptake of heavy metals (HM), as well as finding the most reliable methods for the prediction of availability, continues to be one of the most crucial problems in agricultural and environmental studies. In agricultural soils from two regions in Kosovo, known for its metal pollution, we collected 60 soil and plant samples (wheat, corn, potatoes, and grass). Heavy metals were extracted from soil with aqua regia (pseudototal concentration), NH4OAc‐EDTA (potential bioavailable), and NH4NO3 (mobile fraction), plant samples were digested with HNO3/H2O2 (microwave assisted extraction). The pseudo total content of Cd, Pb, and Zn showed high value in Mitrovice (mean: Cd–2.92, Pb–570.15, and Zn–522.86 mg kg?1), whereas in Drenas region Ni and Cr showed high value with a mean 258.54 and 203.22 mg kg?1. Also, the potential bioavailability and mobile form of these metals were increased in Mitrovice (mean: Cd–1.59, Pb–217.05, Zn–522.86 mg kg?1, respectively Cd–0.17, Pb–0.64, and Zn–15.45 mg kg?1), compared to Drenas. Cd and Pb were elevated in potato tubers (mean Cd–0.48 and Pb–0.85 mg kg?1). The TF was higher for micronutrients (Zn and Cu) than for non‐essential metals (Cd and Pb). Multiple regression analysis showed a good model for prediction of Cd, Pb and Zn content in plant with significance 99.9%, whereas this model was not significant for Cu, Cr, and Ni. Soil pH played a significant role in the content of Cd and Zn in wheat and potato plants. Clay content also showed significance in Cd concentration in wheat and potato plants, while carbon content was significant for Cd in grass plants, as well as for Zn in wheat and grass plants.  相似文献   

5.
The effect of added heavy metals (Cd, Cr, Cu, Ni, Pb and Zn) on the rate of decomposition of glutamic acid was studied in four Dutch soil types in order to determine if such measurements would serve as sensitive indicators of heavy metal pollution in soil. The time required to reach the maximum respiration rate (referred to as the decomposition time) with glutamic acid was linearly related to increasing concentrations of Ni in a sandy loam soil.Changes in decomposition time were measured 18 months after addition of 55, 400 or 1000 mg kg? of Cd, Cr, Cu, Ni, Pb or Zn respectively to sand, silty loam, clay and sandy peat soils. A significant increase in the decomposition time occurred with a concentration of 55 mg kg?1 of Cd, Cu or Zn in the sand soil. At 400mgkg?1 adverse effects in the various soils are distinct. The sensitivity of the decomposition time of glutamic acid as a method to measure soil pollution is discussed.  相似文献   

6.
Periphyton and sediment samples were collected from 12 stations along Bayou d'Inde, a very polluted waterway, in Southwestern Louisiana. The samples were analyzed for Zn, Cu, Pb, Ni, Fe, Cr, Al, Cd, and Ag. When metal concentrations in periphyton or sediment are plotted vs sampling station, the metal distributions clearly indicate a major point source of metals at one station which is located at the mouth of an industrial ditch. Metal levels in periphyton generally parallel those found in surface sediments at the same location, but metal levels in periphyton are generally higher than in sediment from the same location, indicating an enrichment over sediment values. For sediments two types of extraction were investigated using leaching with concentrated HNO3 in a high-pressure decomposition vessel and shaking with 1 N HCl for 2 hr. Both methods correlate well for all metals except Ni, but HNO3 extracted more total metal. Correlations between periphyton and sediment were best for Pb, Fe, and Ag. Poorest correlations were seen for Mn, Ni, and Cd. When periphyton and sediment metal concentrations were normalized to Fe, Mn, and Al, correlation factors for some metals improved while others deteriorated.  相似文献   

7.
An experiment was performed to determine the effects of adding municipal solid waste (MSW) and poultry manure (PM) to a soil polluted with chromium (Cr), lead (Pb), and Cr + Pb on the biological parameters of the soil. Soil was mixed with two solutions of Cr(NO3)3 and/or Pb(NO3)2 to give three concentrations (0, 100, and 250 mg Cr kg?1 soil and 0, 100, and 250 mg Pb kg?1 soil) and treated with MSW or PM. When the soil was contaminated with the metals without combining, the greatest adenosine triphosphate (ATP), urease, and phosphatase inhibition percentages occurred for 250 mg Pb kg?1 soil. When the heavy metals were mixed, the inhibition of the biochemical parameters increased. The application of MSW and PM decreased the inhibition of the biochemical parameters and microbial population in the polluted soils. The inhibition percentage was greater for the soil amended with MSW than with PM, possibly due to the high humic acid concentration.  相似文献   

8.
Current non-invasive biomonitoring techniques to measure heavy metal exposure in free ranging birds using eggs, feathers and guano are problematic because essential metals copper (Cu) and zinc (Zn) deposited in eggs and feathers are under physiological control, feathers accumulate metals from surface contamination and guano may contain faecal metals of mixed bioavailability. This paper reports a new technique of measuring lead (Pb), Cu and Zn in avian urate spheres (AUS), the solid component of avian urine. These metal levels in AUS (theoretically representing the level of metal taken into the bloodstream, i.e. bioavailable to birds) were compared with levels in eggs (yolk and shell), feathers and whole guano from chickens (Gallus gallus domesticus) exposed to a heavy metal-contaminated soil (an allotment soil containing Pb 555?mg?kg?1 dry mass (dm), Cu 273?mg?kg?1?dm and Zn 827?mg?kg?1?dm). The median metal levels (n?=?2) in AUS from chickens exposed to this contaminated soil were Pb 208???g?g?1 uric acid, Cu 66???g?g?1 uric acid and Zn: 526???g?g?1 uric acid. Lead concentrations in egg yolk and shell samples (n?=?3) were below the limit of detection (<2?mg?kg?1), while Cu and Zn were only consistently detected in the yolk, with median values of 3 and 70?mg?kg?1 (dm), respectively, restricting the usefulness of eggs as a biomonitor. Feathers (n?=?4) had median Pb, Cu and Zn levels respectively of 15, 10 and 140?mg?kg?1 (dm), while whole guano samples (n?=?6) were 140, 70 and 230?mg?kg?1 (dm). Control samples were collected from another chicken flock; however, because they had no access to soil and their diet was significantly higher in Cu and Zn, no meaningful comparison was possible. Six months after site remediation, by top soil replacement, the exposed chickens had median Pb, Cu and Zn levels respectively in whole guano (n?=?6) of 30, 20 and 103?mg?kg?1 (dm) and in AUS (n?=?4) of 147, 16 and 85???g?g?1 uric acid. We suggest the persistent high Pb level in AUS was a consequence of bone mobilised for egg production, releasing chronically sequestered Pb deposits into the bloodstream. In contrast, AUS levels of Cu and Zn (metals under homeostatic control and sparingly stored) had declined, reflecting the lower current exposure. However because pre- and post-remediation samples were measured using different methods carried out at different laboratories, such comparisons should be guarded. The present study showed that metals can be measured in AUS, but no assessment could be made of availability or uptake to the birds because tissue and blood samples were not concomitantly analysed. A major short coming of the study was the inappropriate control group, having no access to uncontaminated soil and being fed a different diet to the exposed birds. Furthermore guano and urine analysis should have been carried out on samples from individual birds, so biological (rather than just technical) variation of metal levels could have been determined. Future studies into using AUS for biomonitoring environmental heavy metals must resolve such experimental design issues.  相似文献   

9.
Heavy metal phytoextraction is a soil remediation technique, which makes use of plants in removing contamination from soil. The plants must thus be tolerant to heavy metals, adaptable to soil and climate characteristics, and able to take up large amounts of heavy metals. Most of the high biomass productive plants such as, maize, oat and sunflower are plants, which do not grow in cold climates or need intensive care. In this study three “weed” plants, Borago officinalis; Sinapis alba L. and Phacelia boratus were investigated for their ability to tolerate and accumulate high amounts of Cd and Pb. Pot experiments were performed with soil containing Cd and Pb at concentrations of up to 180 mg kg?1 and 2,400 mg kg?1 respectively. All three plants showed high levels of tolerance. Borago officinalis; and Sinapis alba L. accumulated 109 mg kg?1 and 123 mg kg?1 Cd, respectively at the highest Cd spiked soil concentration. Phacelia boratus reached a Cd concentration of 42 mg kg?1 at a Cd soil concentration of 100 mg kg?1. In the case of Pb, B. officinalis and S. alba L. displayed Pb concentrations of 25 mg kg?1 and 29 mg kg?1, respectively at the highest Pb spiked soil concentration. Although the Pb uptake in P. boratus reached up to 57 mg kg?1 at a Pb spiked soil concentration of 1,200 mg kg?1, it is not suitable for phytoextraction because of its too low biomass.  相似文献   

10.
Abstract

The accumulation of heavy metals in plants is related to concentrations andchemical fractions of the metals in soils. Understanding chemical fractions and availabilities of the metals in soils is necessary for management of the soils. In this study, the concentrations of copper (Cu), cadmium (Cd), lead (Pb), and zinc (Zn) in tea leaves were compared with the total and extractable contents of these heavy metals in 32 surface soil samples collected from different tea plantations in Zhejiang province, China. The five chemical fractions (exchangeable, carbonate‐bound, organic matter‐bound, oxides‐bound, and residual forms) of the metals in the soils were characterized. Five different extraction methods were also used to extract soil labile metals. Total heavy metal contents of the soils ranged from 17.0 to 84.0 mgCukg?1, 0.03 to 1.09 mg Cd kg?1, 3.43 to 31.2 mg Pb kg?1, and 31.0 to 132.0 mg Zn kg?1. The concentrations of exchangeable and carbonate‐bound fractions of the metals depended mainly on the pH, and those of organic matter‐bound, oxides‐bound, and residual forms of the metals were clearly controlled by their total concentrations in the soils. Extractable fractions may be preferable to total metal content as a predictor of bioconcentrations of the metals in both old and mature tea leaves. The metals in the tea leaves appeared to be mostly from the exchangeable fractions. The amount of available metals extracted by 0.01 mol L?1 CaCl2, NH4OAc, and DTPA‐TEA is appropriate extractants for the prediction of metals uptake into tea plants. The results indicate that long‐term plantation of tea can cause sol acidification and elevated concentrations of bioavailable heavy metals in the soil and, hence, aggravate the risk of heavy metals to tea plants.  相似文献   

11.
This paper investigates the pollution load of selected trace elements in 32 soil samples collected around 21 different mining areas of the Iberian Pyrite Belt (Southwest Spain), integrating chemical data with soil parameters to help understand the partitioning and mobility of pollutants. The minesoils are depleted in acid neutralising minerals and show limiting physicochemical properties, including low pH values and very high anomalies of potentially hazardous metals. The total concentrations of As (up to 1,560 mg kg?1) and certain heavy metals (up to 2,874 mg kg?1 Cu, 6,500 mg kg?1 Pb, 6,890 mg kg?1 Zn, 62 mg kg?1 Hg and 22 mg kg?1 Cd) are two orders of magnitude above the soil background values. The close association of Cd and Zn with the carbonate content in lime-amended minesoils suggests metal immobilisation through adsorption and/or co-precipitation mechanisms, after acid neutralisation, whereas As and Pb are similarly partitioned into the soil and mostly associated with iron oxy-hydroxides.  相似文献   

12.

Purpose

Heavy metal distribution in soils is affected by soil aggregate fractionation. This study aimed to demons trate the aggregate-associated heavy metal concentrations and fractionations in “sandy,” “normal,” and “mud” soils from the restored brackish tidal marsh, oil exploitation zone, and tidal mudflat of the Yellow River Delta (YRD), China.

Materials and methods

Soil samples were sieved into the aggregates of >2, 0.25–2, 0.053–0.25, and <0.053 mm to determine the concentrations of exchangeable (F1), carbonate-bound (F2), reducible (F3), organic-bound (F4), and residual fraction (F5) of Cd, Cr, Cu, Ni, Pb, and Zn.

Results and discussion

The 0.25–2 mm aggregates presented the highest concentrations but the lowest mass loadings (4.23–12.18 %) for most metal fractions due to low percentages of 0.25–2 mm aggregates (1.85–3.12 %) in soils. Aggregates <0.053 mm took majority mass loadings of metals in sandy and normal soils (62.04–86.95 %). Most soil aggregates had residual Cr, Cu, Ni, Zn, and reducible Cd, Pb dominated in the total Cd, Cr, Cu, Ni, Pb, and Zn concentrations. Sandy soil contained relatively high F4, especially of Cu (F4) in 0.25–2 mm aggregates (10.22 mg kg?1), which may relate to significantly high organic carbon contents (23.92 g kg?1, P?<?0.05). Normal soil had the highest total concentrations of metals, especially of Cu, Ni, and Pb, which was attributed to the high F3 and F5 in the <0.053 mm aggregates. Although mud soil showed low total concentrations of heavy metals, the relatively high concentrations of bioavailable Cd and Cu resulted from the relatively high Cd (F2) and Cu (F2) in the >2 mm aggregates indicated contribution of carbonates to soil aggregation and metal adsorption in tidal mud flat.

Conclusions

Soil type and aggregate distribution were important factors controlling heavy metal concentration and fractionation in YRD wetland soil. Compared with mud soil, normal soil contained increased concentrations of F5 and F3 of metals in the 0.053–0.25 mm aggregate, and sandy soil contained increased concentrations of bioavailable and total Cr, Ni, and Zn with great contribution of mass loadings in the <0.053 mm aggregate. The results of this study suggested that oil exploitation and wetland restoration activities may influence the retention characteristics of heavy metals in tidal soils through variation of soil type and aggregate fractions.
  相似文献   

13.
Ikem  A.  Egiebor  N. O.  Nyavor  K. 《Water, air, and soil pollution》2003,149(1-4):51-75
The concentrations of trace elements in water, sediment and fish samples from Tuskegee Lake located in Southeastern United States were investigated in this study. The Lake is utilized both as a source for municipal drinking water, and for recreational fishing. The water quality characteristics over two sampling periods, the speciation of metals in the Lake sediments, the risk to water column contamination and levels of heavy metals in largemouth bass (Micropterus salmoides) samples from the Lake were evaluated. The Lake water quality characteristics were mostly below the recommended drinking water standards by the United StatesEnvironmental Protection Agency (US EPA) and the European Union (EU) except for aluminum, iron, manganese and thallium. In addition, the average values of Cr, As, Mn, Zn and Cl- in the water samples analyzed were higher than the respective reference values for fresh water. To study the speciation of metals in the Lake sediments, ten elements (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, V, and Zn) in four grain sizes (< 710 μm – 250 μm, < 250 μm – 75 μm, < 75 μm – 53μm, and < 53 μm) were subjected to sequential extractions. Irrespective of grain size, the elements analyzed were distributed in both the non-residual and residual phases except Ni that was found only in the residual fraction. The potential risk to Lake water contamination was highest downstream (Sites 1 and 2) based on the calculated global contamination factors. From the calculated individual contamination factors, Mn and Pb followed by Zn, Cu, Cr, Co and V posed the highest risk to water contamination. Based on this study, the human health risks for heavy metals in fish caught from Tuskegee Lake are low for now, and irrespective of the source of fish, concentrations of metals in muscle tissues were all below the recommended Food and Agriculture Organization (FAO) maximum limits for Pb (0.5 mg Kg-1), Cd (0.5 mg Kg-1), Cu (30 mg Kg-1), and Zn (30 mg Kg-1) in fish.  相似文献   

14.
Abstract: The fraction distributions of heavy metals have attracted more attention because of the relationship between the toxicity and their speciation. Heavy‐metal fraction distributions in soil contaminated with mine tailings (soil A) and in soil irrigated with mine wastewater (soil B), before and after treatment with disodium ethylenediaminetetraacetic acid (EDTA), were analyzed with Tessier's sequential extraction procedures. The total contents of lead (Pb), cadmium (Cd), copper (Cu), and zinc (Zn) exceeded the maximum permissible levels by 5.1, 33.3, 3.1, and 8.0 times in soil A and by 2.6, 12.0, 0.2, and 1.9 times in soil B, respectively. The results showed that both soils had high levels of heavy‐metal pollution. Although the fractions were found in different distribution before extraction, the residual fraction was found to be the predominant fraction of the four heavy metals. There was a small amount of exchangeable fraction of heavy metals in both contaminated soils. Furthermore, in this study, the extraction efficiencies of Pb, Cd, and Cu were higher than those of Zn. After extraction, the concentrations of exchangeable Pb, Cd, Cu, and Zn increased 84.7 mg·kg?1, 0.3 mg·kg?1, 4.1 mg·kg?1, and 39.9 mg·kg?1 in soil A and 48.7 mg·kg?1, 0.6 mg·kg?1, 2.7 mg·kg?1, and 44.1 mg·kg?1 in soil B, respectively. The concentrations of carbonate, iron and manganese oxides, organic matter, and residue of heavy metals decreased. This implies that EDTA increased metal mobility and bioavailability and may lead to groundwater contamination.  相似文献   

15.

Purpose

The objectives of this study were to explore the influences of pH on the release of Cu, Zn, Cd, Pb, Ni, and Cr in sediments derived from the upstream, middle, and downstream reaches of Dongdagou stream in Gansu Province, Northwest China, and to examine the fractionation changes of heavy metals in the sediments after reaching their release equilibrium under different pH conditions.

Materials and methods

Sediment samples were obtained using a stainless steel grab sampler to collect the uppermost 10 cm of sediment from the channel bed. The pH-dependent release experiment was conducted in the solid-to-liquid ratio of 1:20 at different pH values (2, 4, 6, 8, 10, and 12) at room temperature. The total Cu, Zn, Cd, Pb, Ni, and Cr concentrations in the sediments were digested using an acid digestion mixture (HNO3 + HF + HClO4) in an open system. Metal fractionation of selected sediments was obtained using the Tessier sequential extraction procedure. Heavy metal concentrations in the samples were determined using atomic absorption spectrophotometry.

Results and discussion

The mean concentrations of heavy metals in sediments decreased in the following order: Zn (1676.67 mg kg?1) > Pb (528.65 mg kg?1) > Cu (391.34 mg kg?1) > Cr (53.48 mg kg?1) > Ni (34.27 mg kg?1) > Cd (11.53 mg kg?1). Overall, the solubility of Cu, Zn, Cd, Pb, and Ni decreased with increasing pH, and they were strongly released at pH 2. Moreover, the solubility of Cr increased with increasing pH, and its release was highest at pH 12. After reaching the release equilibrium of heavy metals under different pH conditions, the percentages of organic Cu, Zn, Cd, and Fe-Mn oxyhydroxide Pb decreased, compared to their initial fractions. The residual fractions of Ni and Cr were dominant, regardless of pH.

Conclusions

The average concentrations of Cu, Zn, Cd, and Pb in sediments were highly elevated compared with the soil background values in Gansu Province, China. The results of this pH-dependent release experiment showed that the release behaviors of Cu, Zn, Pb, and Cr followed an asymmetric V-shaped pattern, whereas Cd and Ni followed an irregular L-shaped pattern. The changes in the release of heavy metals in sediments were related to their redistribution between chemical fractionations.
  相似文献   

16.
The main objective of this study was to examine the effectiveness of vermiculite for removing heavy metals from water. Vermiculite components were analyzed by X-ray fluorescence, and the concentrations of metal ions were measured by inductively coupled plasma spectrometry. Serial batch kinetic tests and batch sorption tests were conducted to determine the removal characteristics for heavy metals in aqueous solutions. Solution pH values of tests with the inflated vermiculites generally increased and then stabilized. Equilibrium pH was generally established within 5?h. Removal rates of inflated vermiculite were tested at the initial concentration of 3?mg/L. At equilibrium concentrations, except for chromium (36.23%), most heavy metals were effectively removed (96.08?C98.54%). Finally, sorption data were correlated with both Langmuir and Freundlich isotherms. For each metal, the Q max obtained using the Langmuir isotherm was as follows: lead, 725.4?mg?kg?1; cadmium, 568.8?mg?kg?1; zinc, 540.2?mg?kg?1; copper, 457.2?mg?kg?1; and chromium, 0.9?mg?kg?1. The study results indicate that inflated vermiculite has outstanding removal rates and therefore can be used as an adsorbent for various heavy metals.  相似文献   

17.
沉积物重金属污染是水环境污染评价的重要内容,重金属含量水平常被作为水环境质量的重要指标之一。为了掌握华北平原的府河和白洋淀中沉积物重金属的污染水平,研究了19个沉积物样品和3个土壤样品中7种重金属的污染特征,利用地积累指数法、潜在生态危害指数法及生物效应浓度法评估了重金属的环境风险,并初步分析了污染来源。结果表明,府河和白洋淀沉积物受多种重金属复合污染,其中Zn、Pb、Cu和Cd污染较为严重,府河沉积物的潜在生态环境危害强于白洋淀。相关分析显示府河和白洋淀重金属污染具有相似污染源,保定市工业废水、生活污水及府河沿岸金属冶炼企业很可能是白洋淀地区重金属的主要来源。从城市环境管理、生态环境修复、宣传教育等方面提出白洋淀区域重金属污染控制对策与建议,为白洋淀区域生态环境保护提供科技支撑。  相似文献   

18.
Soils in areas of mining and smelting of Pb–Zn ores in Southern Poland are strongly enriched in heavy metals (Zn, Pb, Fe, Cd, Tl, As). The highest concentrations of Zn (<55,506 mg kg?1), Pb (<8,262 mg kg?1), Cd (<220 mg kg?1) and Tl (<67 mg kg?1) are linked to the fine fractions of upper soil layers in sites contaminated by past exploitation and processing of ores. The high stress of metals, and the negative influence of acid waste drainage has limited the development of flora and fauna in these areas. The increasing ability of plants to grow is due to the positive symbiotic action of fungi and bacteria. The mycorrhizal communities were identified in rhizospheres rich in unstable Zn–Pb–Fe sulphides such as sphalerite, galena, pyrite and marcasite and carbonates of Zn (smithsonite) and Pb (cerussite). They occur in associations with sulphates, e.g., gypsum. In parts of fungi, secondary mineral phases containing Zn, Pb, Fe and Mn occur. Metal-bearing aggregates formed during symbiotic action between myccorhiza and bacteria connected with them. They enhance the binding of bio-available ions of Zn, Pb and Mn in the most unstable phases. Metal contents in the mycorrhizal parts of the rhizospheric soils were determined by Atomic Absorption Spectroscopy. Mineralogical investigations involved X-ray diffraction, scanning electron microscopy with energy dispersive spectrometry.  相似文献   

19.
Sulfuric acid leaching is a promising technique to extract toxic metals from polluted soils. The objective of this study was to define the optimum sulfuric acid leaching conditions for decontamination of the fine particle fraction (<125???m) of an industrial soil polluted by Cd (16.8?mg?kg?1), Cu (3,350?mg?kg?1), Pb (631?mg?kg?1) and Zn (3,010?mg?kg?1). Batch leaching tests in Erlenmeyer shake flasks showed that a soil pulp pH between 1.5 and 2.0 using a solid concentration (SC) ranging from 5 to 20?% is adequate to efficiently solubilize toxic metals. Leaching tests performed at different temperatures (20, 40, 60 and 80?°C) also revealed that it is not beneficial to heat the soil suspension during the leaching treatment. The application in a 1-L stirred tank reactor of five consecutive 1-h leaching steps at 10?% SC and ambient temperature, followed by three water washings steps resulted in the following metal extraction yields: 30?% As, 90?% Cd, 43?% Co, 7?% Cr, 88?% Cu, 75?% Mn, 26?% Ni, 18?% Pb and 86?% Zn. The decontaminated soil conformed to Quebec norms for commercial and industrial use of soil.  相似文献   

20.
The effects of Hg, As, Pb, Cu, Cd, and Cr (1, 2, and 5 mg L?1 each) on Azolla pinnata R. Br. were analyzed. The treatments (2 and 5 mg L?1) of the heavy metal pollutants decreased Hill activity, chlorophyll, protein and dry wt, and increased tissue permeability over control values. The effects were most pronounced with the treatment of 5 mg L?1. The harmful effects of the metals were, in general, found by the treatments in the order: Cd 〉 Hg 〉 Cu 〉 As 〉 Pb 〉 Cr. There was no significant change in these parameters at 1 mg L?1 of the metals over control. Thus Azolla pinnata shows tolerance to the heavy metals tested up to 1 mg L?1 each.  相似文献   

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