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A novel study on using geoelectrical resistivity, soil property, and hydrogeochemical analysis methods for delineating and mapping of heavy metal in aquifer system is presented in this paper. A total of 47 surveys of geoelectrical resistivity with Wenner configuration were conducted to determine the subsurface and the groundwater characteristics. The groundwater sample from 53 existing wells and 2 new wells has been analyzed to derive their water chemical content. The chemical analysis was done on the soil sample obtained from new two wells and from selected locations. The water and soil chemical analysis results from the new two wells were used as calibration in resistivity interpretation. The occurrence of heavy metal in aquifer system was expected to detect using the geoelectrical resistivity survey for the whole study area. The result of groundwater analysis shows that the groundwater sample contains a relatively low concentration of Fe (<?0.3 mg/L) elongating from the south up to the middle region. While in the middle and the northwestern, Fe concentration is relatively high (around 12 mg/L). Chemical analysis of soil sample shows that in the lower resistivity zone (<?18 Ωm), Al and Fe concentrations are comparatively high with an average of 68,000 and 40,000 mg/kg, respectively. Starting from the middle to the northwestern zone, the resistivity value appears to be low. It is definitely caused by higher Al and Fe concentration within the soil, and it is supported also by lower total anion content in the groundwater. While the resistivity value of more than 40 Ωm in aquifers is obtained in the zone which Fe concentration is relatively lower in the soil but not present in the groundwater. Correlation Fe concentration in the soil and Fe concentration in the groundwater sample shows the trend of positively linear; however, the Al concentration in soil has no correlation with Al content in groundwater. Finally, the probability of high heavy metal zone in the aquifer system is easily delineated by the distribution of geoelectrical resistivity presented in depth slice shapes which extend from the Boundary Range Composite Batholith in the north to the northwest.  相似文献   
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Geochemical patterns for elements, such as Sn, W and Au, present in drainage sediments as resistate heavy minerals are often erratic and difficult to interpret. To investigate the source of these problems and develop methods of eliminating them we have compared the behavior of Sn, present as cassiterite, and associated pathfinder elements downstream from a small primary Sn deposit in Perak, Peninsular Malaysia.Dispersion trains for the pathfinder elements are characterized by smooth decay patterns and differences in concentrations between high- and low-energy environments, characterized by coarse-and medium-grained sands respectively, are not significant. In contrast, Sn (and magnetite) concentrations are extremely erratic with significantly higher concentrations in high- compared to low-energy environments. As a result the dispersion train for Sn exhibits no regular decay pattern away from its source. These findings suggest that the action of the stream is analogous to that of sluice box, with light minerals being winnowed away and cassiterite, together with magnetite, accumulating. For all but the finest sizes this process, which is most efficient in high-energy environments, causes considerable local variability in Sn content of the sediments. However, because the hydraulic behavior of cassiterite and magnetite is similar, but magnetite is not associated with the primary mineralization, the Sn/magnetite ratio can be used to eliminate Sn anomalies resulting from local variations in hydraulic conditions.The concept of hydraulic equivalence of cassiterite and magnetite was extended to examining the relationship between Sn and different size fractions of the light minerals that constitute the bulk of most sediments. Greatest contrast is obtained when the Sn content of the −270 mesh (−53 μm) fraction is re-expressed as its hydraulic equivalent concentration in −65 + 100 mesh (−212 + 150 μm) material.For exploration purposes it is concluded that: (1) providing cassiterite is present in the fine size fractions, sampling of this material will reduce hydraulic effects, thereby reducing data variability, and can also increase the length of the anomalous dispersion train; and (2) hydraulic effects can also be reduced by re-expressing Sn concentrations as ratios to magnetite (provided this is not associated with the primary Sn mineralization) or a hydraulically equivalent size fraction of the light minerals that constitute the bulk of the sediment. Similar principles probably apply to the interpretation of geochemical data for other elements dispersed in drainage sediments as heavy minerals; this warrants further investigation.  相似文献   
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新疆阿尔泰克因布拉克铜锌矿床地质特征及成矿作用   总被引:4,自引:1,他引:3  
克因布拉克中型铜锌矿床赋存于早二叠世花岗岩外接触带的上志留统-下泥盆统康布铁堡组黑云石英片岩、变质石英砂岩中。矿床的形成经历了夕卡岩期、热液期和表生期,铜锌矿主要形成于热液期。矿石中石英和方解石流体包裹体划分为H_2O-NaCl型和H_2O-CO_2(±CH_4/N_2)-NaCl型。成矿温度变化于146~448℃,在170℃、270℃和350℃出现峰值;流体盐度变化于0.2%~46.9%NaCl_(eq),峰值为1.5%NaCl_(eq)和5.5%NaCl_(eq);流体的密度0.55~1.19g/cm~3。硫化物的δ~(34)S集中变化于-8.4‰~1.9‰,峰值为0‰,表明硫来自岩浆。石英和方解石δD_(SMOW)介于-130‰~-79‰,δ~(18)O_(SMOW)值介于8.0‰~11.6‰,δ~(18)O_(H2O)值为-1.7‰~4.43‰,表明成矿流体主要是岩浆水,混合大气降水。方解石中δ~(13)C_(PDB)变化于-5.3‰~-1.1‰,暗示碳来自花岗质岩浆。成矿时代为早中二叠世,成矿作用与花岗质岩浆期后的热液活动有关。  相似文献   
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Unfertilizable fruiting buds of mango plant Mangifera Indica L, an agrowaste, is used as a biomass in this study. The efficacy of the biosorbent was tested for the removal of lead, copper, zinc and nickel metal ions using batch experiments in single and binary metal solution under controlled experimental conditions. It is found that metal sorption increases when the equilibrium metal concentration rises. At highest experimental solution concentration used (150 mg/L), the removal of metal ions were 82.76 % for lead, 76.60 % for copper, 63.35 % for zinc and 59.35 % for nickel while at lowest experimental solution concentration (25 mg/L), the removal of metal ions were 92.00% for lead, 86.84 % for copper, 83.96 % for zinc and 82.29 % for nickel. Biosorption equilibrium isotherms were plotted for metal uptake capacity (q) against residual metal concentrations (Cf) in solution. The q versus Cf sorption isotherm relationship was mathematically expressed by Langmuir and Freundlich models. The values of separation factor were between zero and one indicating favourable sorption for four tested metals on the biosorbent. The surface coverage values were approaching unity with increasing solution concentration indicating effectiveness of biosorbent under investigation. The non-living biomass of Mangifera indica L present comparable biosorption capacity for lead, copper, zinc and nickel metal ions with other types of biosorbent materials found in literature and is effective to remove metal ions from single metal solutions as well as in the presence of other co-ions with the main metal of solution.  相似文献   
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In this study, palm shell activated carbon modified with task-specific ionic liquid was used as a novel electrode component for the potentiometric determination of cadmium ions in water samples. The proposed potentiometric sensor has good operating characteristics, including relatively high selectivity towards the Cd (II) ion, a Nernstian response to Cd (II) ions in a working concentration range of 1.0 × 10?9–1.0 × 10?2 M, with a reasonable detection limit of 1 × 10?10 M and a slope of 30.90 ± 1.0 mV/decade. No significant changes in electrode potential were observed when the pH was varied over the range of 4–9. A direct technique based on the use of ion-selective electrode potentiometry has been developed in our laboratory for the study of reaction kinetics and kinetic methods of analysis by continuous monitoring of the rate of production or consumption of an ion. The apparent adsorption rate constant was estimated assuming pseudo-second-order kinetics. Additionally, the proposed electrode has been successfully used for the determination of the cadmium content in real samples without a significant interaction from other cationic or anionic species.  相似文献   
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This study employed three chemometric data mining techniques (factor analysis (FA), cluster analysis (CA), and discriminant analysis (DA)) to identify the latent structure of a water quality (WQ) dataset pertaining to Kinta River (Malaysia) and to classify eight WQ monitoring stations along the river into groups of similar WQ characteristics. FA identified the WQ parameters responsible for variations in Kinta River's WQ and accentuated the roles of weathering and surface runoff in determining the river's WQ. CA grouped the monitoring locations into a cluster of low levels of water pollution (the two uppermost monitoring stations) and another of relatively high levels of river pollution (the mid-, and down-stream stations). DA confirmed these clusters and produced a discriminant function which can predict the cluster membership of new and/or unknown samples. These chemometric techniques highlight the potential for reasonably reducing the number of WQVs and monitoring stations for long-term monitoring purposes.  相似文献   
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The status report on metal pollution in tropical estuaries and coastal waters is important to understand potential environmental health hazards. Detailed baseline measurements were made on physicochemical parameters (pH, temperature, redox potential, electrical conductivity, salinity, dissolved oxygen, total dissolved solid), major ions (Na, Ca, Mg, K, HCO3, Cl, SO4 and NO3) and metals concentrations (27Al, 75As, 138Ba, 9Be, 111Cd, 59Co, 63Cu, 52Cr, 57Fe, 55Mn, 60Ni, 208Pb, 80Se, 66Zn) at estuaries and coastal waters along the Straits of Malacca. Principal component analysis (PCA) was employed to reveal potential pollution sources. Seven principal components were extracted with relation to pollution contribution from minerals-related parameters, natural and anthropogenic sources. The output from this study will generate a profound understanding on the metal pollution status and pollution risk of the estuaries and coastal system.  相似文献   
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This paper aims at determining of inorganic leachate contamination for a capped unsanitary landfill in the absence of hydrogeological data. The 2D geoelectrical resistivity imaging, soil physicochemical characterization, and surface water analysis were used to determine contamination load and extent of selective heavy metal contamination underneath the landfill. The positions of the contaminated subsoil and groundwater were successfully delineated in terms of low resistivity leachate plumes of <10 Ωm. Leachate migration towards the reach of Kelang River could be clearly identified from the resistivity results and elevated concentrations of Fe in the river downslope toe of the site. Concentration of Fe, Mn, Ca, Na, K, Mg, Cu, Cr, Co, Ni, Zn, and Pb was measured for the subsoil samples collected at the downslope (BKD), upslope (BKU), and the soil-waste interface (BKI), of the landfill. The concentration levels obtained for most of the analyzed heavy metals significantly exceed the normal range in typical municipal solid waste landfill sites. The measured heavy metal contamination load in the subsoil is in the following order Fe ? Mn > Zn > Pb > Cr > Cu. Taking into consideration poor physical and chemical characteristics of the local soil, these metals first seem to be attenuated naturally at near surface then remobilize unavoidably due to the soil acidic environment (pH 4.2-6.18) which in turn, may allow an easy washing of these metals in contact with the shallow groundwater table during the periodic fluctuation of the Kelang River. These heavy metals are believed to have originated from hazardous industrial waste that might have been illegally dumped at the site.  相似文献   
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