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1.
The effects of fertilizer applications on runoff loss of phosphorus   总被引：4，自引：0，他引：4  
The phosphorus index (PI) can be used to effectively identify areas with high risks of phosphorus losses. Manures and fertilizers are important source factors for the establishment of the PI system. An artificial precipitation experiment was performed to evaluate phosphorus losses with the applications of different types of fertilizers and manures. The results showed that the total phosphorus (TP) losses in runoff followed the order of ammonium phosphate monobasic (NH4H2PO4), ammonium hydrogen phosphate ((NH4)2HPO4), monobasic potassium phosphate (KH2PO4), chicken manure, and cattle manure with surface application of these fertilizers and manures. The order was slightly changed to NH4H2PO4, KH2PO4, (NH4)2HPO4, chicken manure, and cattle manure with incorporation application under the same rainfall condition. Both the methods and the rate of manure application can affect the amounts of phosphorus in water and particles of runoff. More than 90 % of TP in runoff were lost through suspended particles. Manure application had a significant contribution to the P load in runoff.  相似文献   

2.
This study investigated the effect of cations and anions on the sorption and desorption of iron (Fe) and manganese (Mn) in six surface calcareous soil samples from Western Iran. Six 10 mM electrolyte background solutions were used in the study, i.e., KCl, KNO3, KH2PO4, Ca(NO3)2, NaNO3, and NH4NO3. NH4NO3 and NaNO3 increased the soil retention of Fe and Mn, whereas Ca(NO3)2 decreased the soil retention of Fe and Mn. Iron and Mn sorption was decreased by NO3 ? compared with H2PO4 ? or Cl?. The Freundlich equation adequately described Fe and Mn adsorption, with all background electrolytes. The Freundlich distribution coefficient (K F) decreased in the order H2PO4 ? > Cl? > NO3 ? for Mn and H2PO4 ? > NO3 ? > Cl? for Fe. The highest sorption reversibility was for Fe and Mn in competition with a Ca2+ background, indicating the high mobility of these two cations. A MINTEQ speciation solubility model showed that Fe and Mn speciation was considerably affected by the electrolyte background used. Saturation indices indicated that all ion background solutions were saturated with respect to siderite and vivianite at low and high Fe concentrations. All ion background solutions were saturated with respect to MnCO3(am), MnHPO4, and rhodochrosite at low and high Mn concentrations. The hysteresis indices (HI) obtained for the different ion backgrounds were regressed on soil properties indicating that silt, clay, sand, and electrical conductivity (EC) were the most important soil properties influencing Fe adsorption, while cation exchange capacity (CEC), organic matter (OM), and Mn-DTPA affected Mn adsorption in these soils.  相似文献   

3.
We examined the relationship between soil oxidation capacity and extractable soil manganese, iron oxides, and other soil properties. The Korean soils examined in this study exhibited low to medium Cr oxidation capacities, oxidizing 0.00–0.47 mmol/kg, except for TG-4 soils, which had the highest capacity for oxidizing added Cr(III) [>1.01 mmol/kg of oxidized Cr(VI)]. TG and US soils, with high Mn contents, had relatively high oxidation capacities. The Mn amounts extracted by dithionite-citrate-bicarbonate (DCB) (Mnd), NH2OH·HCl (Mnh), and hydroquinone (Mnr) were generally very similar, except for the YS1 soils, and were well correlated. Only small proportions of either total Mn or DCB-extractable Mn were extracted by NH2OH·HCl and hydroquinone in the YS1 soils, suggesting inclusion of NH2OH·HCl and hydroquinone-resistant Mn oxides, because these extractants are weaker reductants than DCB. No Cr oxidation test results were closely related to total Mn concentrations, but Mnd, Mnh, and Mnr showed a relatively high correlation with the Cr tests (r = 0.655–0.851; P < 0.01). The concentrations of Mnd and Mnh were better correlated with the Cr oxidation tests than was the Mnr concentration, suggesting that the oxidation capacity of our soil samples can be better explained by Mnd and Mnh than by Mnr. The first component in principal components analysis indicated that extractable soil Mn was a main factor controlling net Cr oxidation in the soils. Total soil Mn, Fe oxides, and the clay fraction are crucial for predicting the mobility of pollutants and heavy metals in soils. The second principal component indicated that the presence of Fe oxides in soils had a significant relationship with the clay fraction and total Mn oxide, and was also related to heavy-metal concentrations (Zn, Cd, and Cu, but not Pb).  相似文献   

4.
In order to determine the metal-bearing phases with special emphasis on Cu, a sequential extraction has been carried out on seven soil samples from a sulphide-bearing spodosol profile in Liikavaara Östra, close to the Aitik Copper Mine in northern Sweden. A reference spodosol profile with very low abundances of sulphides located far from anthropogenic emissions was also studied. Five fractions were selected for the extraction: (I) CH3COONa-extractable (exchangeable/adsorbed/carbonate); (II) Na4P2O7-extractable (labile organics); (III) 0.25 M NH2OH·HCl-extractable (amorphous Fe oxyhydroxides/Mn oxides); (IV) 1 M NH2OH·HCl-extractable (crystalline Fe oxides); and (V) KClO3/HCl-extractable (organics and sulphides). The distribution of trace elements (Co, Cr, Cu, Ni, Pb and Zn) in the profile in Liikavaara Östra is different from that in the reference profile. Possible explanations for these differences are (i) the presence of sulphides in the soil, (ii) atmospheric deposition of dust derived from mining activities at the Aitik Copper Mine, and (iii) mineralogical heterogeneities inherited from the deposition of the till. There is no straightforward correlation between the amount of the extracted phases and the metal extractability in the soils. This fact indicates that other factors are important for the retention of trace metals as well. The data presented in this study suggest that Co, Cr and Ni, to a fairly large extent, are associated with the organic matter in the B-horizon in both profiles, while in the C-horizon in Liikavaara Östra, sulphides are probably the more important carriers of these elements. For Co and Ni, Fe oxyhydroxides seem to be important. Most of the Cr occurred in the residual remaining after the leaching procedure. Copper and Zn seem to be associated with the organic matter to some extent in the B-horizon. The concentration of Cu in the C-horizon in Liikavaara Östra is high (2310 ppm), but only a very small fraction is likely to be hosted by sulphides. It is concluded that the major part of Cu in the C-horizon and a prominent fraction in the B-horizon in Liikavaara Östra are associated with some secondary phase that is extractable during extractions III and IV. Possible candidates for this phase are goethite and inclusions of native Cu in weathered biotite.  相似文献   

5.
Mobility of heavy metals from coal fly ash   总被引：7，自引：0，他引：7  
The mobility of Cd, Co, Cu, Ni, Pb, Sb, and Zn from six different coal-fired power plant fly ashes that show a wide compositional range was examined using a sequential extraction procedure in order to assess their mobility when these wastes are ponded or landfilled. The extraction sequence was as follows: (1) water extractable, (2) cation exchangeable (CH3COONH4 at pH 7), (3) surface oxide-bound cations (CH3COONH4 at pH 5), (4) Fe oxide-bound cations (HONH3Cl), and (5) residual (HF, HCl, HNO3, 211). The heavy metal contents in the extraction solutions were determined by anodic (Cd, Cu, Pb, Sb, and Zn) and cathodic (Ni and Co) stripping voltammetry. The results reveal differences in the total contents of the selected trace elements among the fly ash samples, which must be related to differences in coal composition and combustion technology. The extractable fraction under natural conditions ranges from 1.5 to 36.4 percent of the total element content. Cadmium, Co, Cu, and Zn show the highest extractable fraction (10.8–18.9 percent on average). Cadmium is the most easily water-extractable element, while Co, Cu, and Zn increase their mobility as the severity of the extraction increases. Cobalt, Ni, Pb, and Zn are mainly associated with the surface oxide-bound and Fe oxide-bound fractions. Nickel, Pb, and Sb have low mobility potentials (5.3–6.6 percent as extractable fraction), but Sb presents a relatively high water-extractable fraction.  相似文献   

6.
Various extraction procedures were employed for measuring extractable concentrations of potential toxic elements in soil. The extractability of Cd, Cu, Pb and Zn in four contaminated and four non-contaminated soils of Japan, was compared by single extraction (CaCl2, DTPA, NH4Cl, 0.1 M HCl and 1 M HCl ) and sequential extraction procedures [(six operationally defined chemical phases, viz. water soluble (Fl), exchangeable (F2), carbonate (F3), oxide (F4), organic (F5) and residual (F6) fractions)]. Extractability of metals from soils samples varied depending on metals and/or extradants used. Among the extradants, 1 M HCl extracted the largest proportion of Cd (79 to 96% of total), Cu (61 to 83%), Pb (51 to 99%) and Zn (23 to 52%) from soils followed by 0.1 M HCl, NH4Cl, DTPA and CaCl2. In all the extradants, the proportion of extractability of metals was higher in the contaminated soils than the non-contaminated soils. Regardless of soils and extradants, relative extractability was higher for Cd as compared to other three metals. The use of 1 M HCl may be recommended for first-level screening of soil contamination with heavy metals. The other four weak extradants are believed to provide a better assessment of bioavailable/mobile metals content in soils than 1 M HCl extradant. However, 0.1 M HCl mobilized all four metals irrespective of soil types, therefore, might be the best choice if only one extradant is to be used. The sequential extraction procedures showed 22 to 64% of total Cd was in the mobile fraction (sum of Fl to F3), while the corresponding values for Cu, Pb and Zn in this fractions were 2 to 23% suggesting higher mobility of Cd than other three metals. The single extraction procedures are simple and easy to perform and obtained results are comparable with sequential extraction procedure.  相似文献   

7.
Near-surface atmospheric dust in Changsha city of China was analyzed in terms of morphological and geochemical composition. Morphological and chemical composition of the dust particles were analyzed by environmental scanning electron microscopy coupled with an energy-dispersive X-ray analyzer. Results indicated that the atmospheric dusts were mainly composed of spherule, plate, irregularly shaped and agglomerate, which contains variable sizes and amounts of particles. The dust particles could be categorized into five groups based on their chemical characteristic: Al-, Si-, Ca-, C-rich particles and aggregate. These particles and aggregate could be directly related to nearby polluting activities, such as building construction, traffic emission and coal combustion. The X-ray diffraction results show that the main minerals for atmospheric dust are gypsum, quartz and calcite. Mica, halloysite, montmorillonite, hematite, brushite, zeolite, sepiolite, feldspar, alite, dickite, SiS2, Fe6(OH)2CO3, FeSO4, CdSO4, Pb(NO)2O3, Al2SO4(OH)4, As2O3SO3, (NH4)2SO4, NH4Cl, K(NH4)·Ca(SO4)2·H2O are also detected in samples. The identification of heavy metals shows that the concentrations of Cr (403.5?mg?kg?1), Cu (126?mg?kg?1), Zn (1541.5?mg?kg?1), Cd (2.5?mg?kg?1) and Pb (348?mg?kg?1) in the atmospheric dust are much higher compared to background value of soil. It indicates that the heavy metal (Cr, Cu, Zn, Cd and Pb) in the atmospheric dust is mainly due to human activities. The identification of main sources of atmospheric dust collected in typical areas can help to control the polluting sources in urban area.  相似文献   

8.
This study analyses the adsorption of Pb(II) and Cr(III) in soils. These metals are commonly found together in nature in urban wastes or industrial spillages, and the theoretical approach of the work was to evaluate the response of the soil to continuous Cr and Pb spillages to soil in terms of several physicochemical parameters. The influence of an anthropogenic input of phosphorus was evaluated. Continuous flow experiments were run in duplicates in acrylic columns (25 cm × 3.2 cm). The influent Cr(III) and Pb(II) solutions of 10 mg l?1 and 25 mg l?1 at pH 5 were pumped upward through the bottom of the columns to ensure saturation flow conditions. Also, successive experiments were run with the above concentrations of Cr(III) and Pb(II) and NaH2PO4, keeping metal to phosphorus ratio of 1:0, 1:0.1 and 1:1. Modelling parameters included Freundlich and Langmuir equations, together with the Two-site adsorption model using CXTFIT code. Results obtained allowed concluding that Pb(II) adsorption presents a certain degree of irreversibility and the continued spillages over soil increment the fraction which is not easily desorbed. Cr(III) desorption was almost complete, evidencing its high mobility in nature. The presence of an anthropogenic input of phosphorus leads to a marked increase of both Pb(II) and Cr(III) adsorption in soils. Z-potential measurements allow to discard the electrostatic attraction of Cr(III) and Pb(II) with the surface charged soil as the dominant process of metal sorption. Instead, CheaqsPro simulation allows to identify PbH2PO4 +, PbHPO4 (aq) and CrHPO4 + as the dominant species which regulate Cr(III) and Pb(II) transport in soils.  相似文献   

9.
鲁照玲  胡红云  姚洪 《岩矿测试》2012,31(2):241-246
分别采用HNO3-HF、HNO3-HF-HCl和HNO3-HF-H2O2三种消解体系,通过微波和PTFE密封罐电热板对土壤标准物质进行前处理,采用电感耦合等离子体质谱(ICP-MS)对样品中的重金属元素Cr、Ni、Cu、Zn、As、Cd和Pb进行定量分析。探讨了前处理试剂(主要为HNO3、HCl和HF)以及土壤基体效应对Cr、Ni、Cu、Zn、As、Cd和Pb定量分析的影响。研究结果表明,前处理试剂对Cr、Ni、Cu、Zn、As、Cd和Pb的定量分析具有不同程度的影响;对于土壤基体,在三种消解体系下均可观察到基体抑制效应;采用PTFE密封罐电热板消解方法前处理,待测元素及相同元素不同同位素的方法空白和检出限均较低,效果整体优于微波消解法。特别是HNO3-HF-HCl消解体系,通过选用52Cr、60Ni、65Cu、66Zn、75As和206Pb等同位素,重金属元素Cr、Ni、Cu、Zn、As、Cd和Pb的测定值均能保证在标准值的允许误差范围内,可以满足大批量土壤样品中重金属元素同时定量分析的需要,为高效准确地开展土壤的风险评估以及为土壤的修复治理提供科学依据。  相似文献   

10.
We studied the states of rare earth elements in ore of the Xianglushan rare earth deposit. Rare earth ore samples were tested and examined by scanning electron microscope, electron probe, and chemical leaching. No independent rare earth minerals were detected by scanning electron microscope. Elements detected by the electronic probe for the in situ micro-zone of the sample included: O, Al, Si, Ca, Mg, Fe, Ti, K, Na, S, Cl, C, Cu, Cr, V, and Pt. Rare earth elements were not detected by electron probe. (NH4)2SO4, (NH4)Cl, NaCl, and H2SO4 were used as reagents in chemical leaching experiments that easily leached out rare earth elements under the action of 10% reagent, indicating that the rare earth elements in ore are mainly in the ionic state rather than present as rare earth minerals.  相似文献   

11.
A novel complex continuous system of solid solutions involving vauquelinite Pb2Cu(CrO4)(PO4)(OH), bushmakinite Pb2Al(VO4)(PO4)(OH), ferribushmakinite Pb2Fe3+(VO4)(PO4)(OH), and a phase with the endmember formula Pb2Cu(VO4)(PO4)(H2O) or Pb2Cu(VO4)(РО3ОН)(ОН) is studied based on samples from the oxidation zone of the Berezovskoe, Trebiat, and Pervomaisko-Zverevsky deposits in the Urals, Russia. This is the first natural system in which chromate and vanadate anions show a wide range of substitutions and the most extensive solid solution system involving (CrO4)2– found in nature. The major couple substitution is Cr6+ + Cu2+ ? V5+ + M3+, where M = Fe, Al. The correlation coefficients calculated from 125 point analyses are: 0.96 between V and (Fe + Al), 0.96 between Cr and (Cu + Zn),–0.96 between V and (Cu + Zn),–0.97 between Cr and (Fe + Al), and–0.97 between (Fe + Al) and (Cu + Zn). The substitutions V5+ ? Cr6+ (correlation coefficient–0.98) and to a lesser extent P5+ ? As5+ (correlation coefficient–0.86) occur at two types of tetrahedral sites, whereas the metal–nonmetal/metalloid substitutions, i.e., V or Cr for P or As, are minor. The substitution Fe3+ ? Al3+ is also negligible in this solid solution system.  相似文献   

12.
The aim of the study was to determine whether the application of phosphate compounds (phosphorite rock, phosphate fertilizer) to polyminerallic waste rocks can inhibit sulfide oxidation and metal mobility (Cu, Pb, Zn, Cd, Ni, Mn, Mg). Waste rocks comprised sulfidic carbonaceous shales and were sourced from the Century Pb-Zn mine, NW Queensland, Australia. The acid producing, Pb-Zn rich rocks consisted of major quartz, muscovite/illite, dolomite, siderite and kaolinite as well as smaller amounts of sulfide minerals (e.g. galena, sphalerite, pyrite). Laboratory leach experiments were conducted on finely granulated phosphate-treated waste rocks (>2 to <30 mm) over 13 weeks, whereas phosphate amendment of coarsely granulated waste rocks (sand to boulder size) was investigated using heap leach piles at the mine site over an 11 months period. Results of the laboratory experiments demonstrate that the treatment of finely granulated waste rocks with phosphorite rock produced leachates with near-neutral pH values due to calcite dissolution. This in turn did not allow the leaching of apatite, formation of secondary phosphate phases and phosphate stabilization to occur. Metal mobility in these amended wastes was restricted by the dissolution of calcite and the resultant near-neutral pH conditions. By contrast, the application of the water-soluble phosphate fertilizer MKP (KH2PO4) to polyminerallic sulfidic waste rocks during the short-term laboratory experiments led to the formation of phosphate coatings and precipitates and inhibited acid and metal release (Cd, Mn, Ni, Pb, Zn). At least in the short term, the application of phosphate fertilizers proved to be an effective method. However, results of the long-term field trials demonstrate that coarsely granulated waste rocks were not coated by secondary phosphate phases and that amendment by phosphorite rock or superphosphate fertilizer did not improve leachate quality compared to the unamended waste. Thus, phosphate stabilization appears ineffective in suppressing oxidation of sulfides in coarsely granulated mine wastes.  相似文献   

13.
 Selenium (Se), an animal toxicant and aquifer contaminant, occurs in coal mine environments of Wyoming. There is a paucity of information on solution-phase Se speciation in mine soils. The objectives of this study were to compare Se extraction efficiencies of various reagents and to characterize SeO2– 3 (selenite), SeO2– 4 (selenate) and organic Se components in these extracts. Forty coal mine soils were extracted using DI (deionized) water, hot water (0.1% CaCl2), AB-DTPA, NaOH, and KH2PO4. Each solution was analyzed for total dissolved Se, and inorganic and organic Se fractions. Both inorganic and organic Se fractions were detected in the soil extracts. The order of Se (total, inorganic, and organic) extraction efficiency for different reagents was DI water < hot water < AB-DTPA < NaOH < KH2PO4. The inorganic–organic Se ratios in DI water, hot water, AB-DTPA, NaOH, and KH2PO4 extracts were 60 : 40, 26 : 74, 61 : 39, 87 : 13, and 52 : 48, respectively, indicating predominance of inorganic Se in all but the hot water extract. Selenite was the dominant inorganic species in AB-DTPA and KH2PO4 extracts, while SeO2– 4 was the major Se species in the DI water, hot water, and NaOH extracts. Significant correlations (P<0.01) were observed among extractable inorganic Se [NaOH and KH2PO4 (r=0.95); hot water and AB-DTPA (r=0.89)], total soluble Se [DI water with hot water (r=0.98) and AB-DTPA (r=0.95)], and Se species [SeO2– 3 in AB-DTPA with SeO2– 4 in NaOH (r=0.94) and SeO2– 3 in KH2PO4 (r=0.88)]. These correlations are indicative of Se extraction efficiency, thermodynamically predicted chemical transformations (such as oxidation of SeO2– 3 to SeO2– 4), and probable interconversions between the organic and inorganic Se fractions (r=0.70 in KH2PO4 extracts); as a whole the correlations can be used as statistical validations of possible geochemical processes. Received: 21 August 1995 · Accepted: 16 October 1995  相似文献   

14.
Heavy metal distribution in karst soils from Croatia and Slovakia   总被引：1，自引：1，他引：0  
With the use of the optimised three-step BCR sequential-extraction procedure it was possible to assess the mobility of selected elements in soil profiles from Croatian and Slovakian karst terrains. The soils in the Croatian karst were enriched in Cr, Ni, V, Mn, Cu, Cd and Mo, while soils from the Slovak Karst had high Pb and Zn concentrations. It was determined that the elements were most readily mobilised from the topsoil and the degree of mobility decreased with depth. Cr and Ni were mainly bound to the residual fraction, and Pb in the oxidisable fraction. Cu mobility was high in samples treated with agrochemicals throughout the soil profile.  相似文献   

15.
An understanding of the biogeochemical behaviour of metals in mine spoil materials is a prerequisite to rehabilitate Ni mining sites. The objective of this study was to characterize the fate of metals in different Ni ore spoil materials as influenced by hydrological conditions and fertilisation practices. In tropical ultramafic complexes, the different stages of lateritic weathering lead to two types of ores, and therefore, to two spoil types. They are mainly either a clay-rich saprolite, so-called “garnierite”, enriched in phyllosilicates, or a limonitic material, enriched in Fe oxides. Lysimeter columns were designed to monitor leaching waters through both spoil materials. The garnieritic spoil released higher concentrations of Mg (mean = 2.25 mg L−1), Ni (0.39 mg L−1) and Cr (1.19 mg L−1) than the limonitic spoil (Mg = 0.5 mg L−1; Ni = 0.03 mg L−1 and Cr = 0.25 mg L−1). Chromium was mainly in an anionic form in leaching solutions. As exchangeable pools of Cr(VI) in limonite (980 mg kg−1 of KH2PO4-extractable Cr) are considerable its release in water may still occur in the case of a pH increase. In mixed spoil, metal concentrations were almost as low as in the limonitic one. The effect of mineral-N fertilisation was a strong release of cations (Ni, Mg) into the leachate. Phosphate amendment did not affect the soil solution composition under experimental conditions.  相似文献   

16.
Olivine-related (Ni, Mg)3(PO4)2 solid solutions were prepared and equilibrated at 1070 K. Accurate monoclinic unit cell dimensions were determined from Guinier-Hägg photographic data. Structural refinements based on the X-ray profile-fitting technique after Rietveld were carried out for pure nickel (II) orthophosphate and for three Ni/Mg solid solutions. (Ni1-x Mg x )3(PO4)2 phases with 0.40≦x≦0.60 are probably isostructural with Ni3(PO4)2 (P21/a) while phases with low magnesium contents (<27 atom % Mg) deviate structurally from Ni3(PO4)2. The results also show that Ni2+ is partially ordered at the octahedralM(1) sites, withK D (Ni, Mg)=4.0±0.2  相似文献   

17.
The charged sites on soil particles are important for the retention/adsorption of metals. Metallic counterions can neutralize the intrinsic charges on the surfaces of soil particles by forming complexes. In this study, efforts have been made to determine the effect of surface potential, pH, and ionic strength on the adsorption of four metal ions, hexavalent chromium Cr(VI), trivalent chromium Cr(III), nickel Ni(II) and cadmium Cd(II), in glacial till soil. Batch tests were performed to determine the effect of pH (2–12) and ionic strength (0.001–0.1 M KCl) on zeta potential of the glacial till soil. The point of zero charge (pH PZC ) of glacial till was found to be 7.0±2.5. Surface charge experiments revealed the high buffering capacity of the glacial till. Batch adsorption experiments were conducted at natural pH (8.2) using various concentrations of selected metals. The adsorption data was described by the Freundlich adsorption model. Overall glacial till shows lower adsorption affinity to Cr(VI) as compared to cationic metals, Cr(III), Ni(II) and Cd(II).  相似文献   

18.
The study described herein concerns the application of selective chemical extractions on metal-bearing minerals and soils to geochemical exploration. Specifically, the study aims at the detection of anomalous soils in the vicinity of two mineralized zones in Southern Portugal.A kinetic study of the selectivity of partial chemical extractions applied to Cu minerals has been carried out in order to establish a systematic procedure (reagents, extraction plateau, etc.) which could be recommended for soils of the two study zones. It is shown that: (1) NH4 acetate dissolves malachite, azurite and cuprite completely and chrysocolla, conicalcite and atacamite only partially; (2) hydroxylamine hydrochloride dissolves chrysocolla and conicalcite only partially; (3) H2O2 dissolves chalcopyrite only partially; (4) NH4 oxalate (U.V.) dissolves conicalcite and atacamite only partially; (5) mixed-acid attack dissolves residual chalcopyrite, chrysocolla, atacamite and conicalcite.A total of 740 soil samples were collected from the Salgadinho and Tinoca areas. The Cu mineralization in the Salgadinho area is situated in an Upper-Devonian Volcanic-Siliceous Complex. The weathering products of the mineralization are mainly amorphous iron oxides, goethite and hematite. The Cu mineralization in Tinoca area is located in the Arronches-Campo Maior belt, where stratiform Cu mineralization is found. The weathering products of the mineralization are mainly malachite, amorphous iron oxides, goethite and hematite.In order to identify the Cu-bearing phases and the extraction plateau, the −80 mesh fraction of two soil samples was submitted to an extraction procedure using the following reagents in sequence: NH4 acetate, hydroxylamine hydrochloride, NH4 oxalate (dark), NH4 oxalate (U.V.) and finally strong acids.In soils from the Salgadinho and Tinoca areas, the use of NH4 oxalate (U.V.) in single dissolution which would incorporate those phases dissolved by NH4 acetate and NH4 oxalate (dark), gives the broadest anomalous surface and higher contrast for Cu than acid digestion. The analysis of NH4 oxalate (U.V.) extractions, instead of acid digestion, can thus be recommended for both areas.  相似文献   

19.
Heavy metal contamination was the main environmental problem around the Jinchang Ni–Cu mine area of Gansu, Northwest China. The concentration of heavy metals (Cr, Cu, Ni, Pb, and Zn) in various environmental mediums around the Jinchang Ni–Cu mine area were analyzed using atomic absorption spectrometry (AAS). The different chemical speciation of heavy metals was extracted using BCR (European Community Bureau of Reference) sequential extraction procedure, and the concentration of chemical speciation of each heavy metal was measured by inductively coupled plasma-atomic emission spectrometry. The results showed that Cu and Ni were the most important heavy metal pollutants in various mediums including cultivated soils, dust on slagheap surfaces, tailings, and sediments in waste water drains. In the tailings and sediments, the concentrations of Ni were obviously higher than those of Cu, whereas, in the soil and dust, the concentrations of Cu were higher than those of Ni. Analysis of chemical speciation indicated that Cr and Zn were mainly in residual fraction; Cu was mainly in oxidizable fraction; Ni was mainly in reducible fraction and acid soluble fraction; and Pb was mainly in reducible fraction and residual fraction. The extent of contamination of various environmental mediums was different because the heavy metals were derived from different sources. Furthermore, the mobility of various heavy metals was different because of the different distribution of chemical speciation.  相似文献   

20.
A lake sediment core from Vermillion Lake, Sudbury, Ontario was tightly sampled and analyzed for a wide range of trace elements as well as for Pb isotopes. The data resolve multiple historical events in the 140-a history of logging and mining in the Sudbury area in unprecedented detail. Lead-210 data, 137Cs activity and historical information on the start of anthropogenic activities in the Sudbury area were combined to derive an age model for the sedimentary column. Using the age information, it is possible to identify sediment sections enriched and depleted in trace metal(loid)s, particularly Ni and Cu, the two most relevant metals in the Sudbury area. Maxima and minima in the chronology of Ni and Cu coincide well with local production values for both elements until environmental regulations in the 1990s resulted in a decrease in their emission and drainage into Vermillion Lake. Differences in the deposition rates of Ni and Cu, trace-metal distribution patterns throughout the sedimentary column, Pb-isotope data, and comparison with data for local rocks and ores in the Sudbury area were used to identify the sources of pollutants in the early and late periods of mining activities. In addition, the environmental impact on the sediment itself was also studied via the variation of water content and organic matter. Finally, a surficial Fe–Mn-enriched layer with elevated concentrations of the oxy-anions (PO4)3−, (AsO4)4−, and (MoO4)2− was identified. This can be distinguished from accumulation of Zn and an increase in the Y / Ho ratio in the upper core sections, which likely imply increasing drainage of fertilizers into the Vermillion River watershed. The chemistry, mineralogy, and isotope composition of the Vermillion Lake sediment column thus contain a very detailed >140-a account of initial severe anthropogenic disturbance, the efforts of remediation and the effects of changing land use towards agricultural and recreational activities.  相似文献   

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