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1.
The leaching of coal and coal/asphaltite/wood-ashes in sulfuric acid (pH 1.0, 25 °C, S/L, 1:10) was studied as a function of time; acid consumption and extracted metal concentrations are presented. Whole coals consumed acid rapidly during the first few minutes, followed by slow acid consumption. Wood-, lignite-, and asphaltite-ashes consumed acid in two stages, the rapid phase extending < 30 min and the slow phase extended up to 10 days. The rapid phase was dominated by the dissolution of Ca, K and Mg ions for wood-ash, by Ca, Al and Mg ions for lignite-ash and Ca and Mg ions for asphaltite-ash. The sulfur concentration in solution and the concentrations of Ca, Fe, K, Mg, Na, P, Al and Mn in the aqueous phase verified the neutralizing capacity of the untreated ashes as well as the formation of insoluble sulfates in the residues. The slow phase kinetics differed for different fuels and exhibited leaching of several abundant elements—Fe, Al, K, Na and Mn. Trace elements (Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, Th, U, V, Zn) sometimes required up to 32 h for maximal extraction from ashes. Suggestions are presented regarding the chemical nature of trace elements in the untreated coals and ashes and suitable residence times for economical industrial processes. We think it possible to combine bacteriological oxidation of sulfidic concentrates of acid leaching from ash of various qualities or even whole coals.  相似文献   

2.
Using a modified extraction procedure, the effect of pH on the leaching of selected elements from Ca-rich (Type C) power plant fly ash was studied. Continuous additions of acetic acid were used to maintain pH values of fly ash slurries at 4.0, 6.0 and 8.0 for 24 h and an additional set was leached at its natural pH (average 11.8) value. Analyses for Se, As, Ca, Cd, Cr, Fe, Na and Pb showed that the highest concentrations occur in the leachate at pH 4.0 and decline with increasing pH. Concentrations of Cr and Fe increased slightly between neutral and high pH. Arsenic, Cd, Cr, Pb and Se concentrations exceeded the Environmental Protection Agency's toxicity criteria at pH 4.0. Selenium was above its toxicity level at pH values near 7 but the other elements were below their respective toxicity levels near neutral pH. Because recent studies show adverse effects of Se on aquatic life at far lower concentrations than the current Environmental Protection Agency's standard, high-Ca, power plant fly ashes represent a potentially hazardous pollutant to surface and subsurface waters.  相似文献   

3.
Seyitömer power plant comprises 4.8% of Turkey's total energy production. The fly ash produced has been deposited in the area, since the 1960s, by a dry disposal technique. In 1997, wet disposal was improperly exercised in the area causing ash flow over agricultural fields. This study is concerned with the chemical analysis of ash, soil and water samples collected in the area following ash-removal studies after the ash flow in 1997. The results reveal that Na, K, Ca, Mg, Mn, Al, Fe, Co, and Cr contents of soil and water are governed by basement lithology in the area, whereas Cd, Pb, Zn, and Cu contents are determined by fly ash from disposal sites. Although lithogenic Cr and Co contents are exceedingly high, comparison with the regulatory standards for drinking water, irrigation water and agricultural soils reveals no pollution pertinent to solid waste production in waters, whereas there is moderate pollution by Pb and Cu in soils.  相似文献   

4.
The leaching of major species from fly ash is a function of the pH of the solution in contact with the fly ash. The aim of this study was to determine the effect of the pH of the leachant on the leaching of species from the ash residues recovered after the long-term fly ash–brine interactions. Acid neutralization capacity (ANC) tests using solutions of different pH values ranging from the initial pH of the ash residues (11–12) to pH 4 were employed in the leaching experiments. The ANC tests revealed that the release of major species from the ash residues depended on the pH of the leachants except for Na and Cl, where the significant concentrations leached were independent of the solution pH. The concentrations of Al and Si in the ANC leachates were very high at pH below 6 while Ca, K, Sr, Mg and B were immediately mobilized from the brine impacted fly ash when in contact with de-ionized water, and leaching increased as the pH decreased. The concentration of SO4 leached from the brine impacted ash residues at high pH was high, and the leaching increased with decrease in the pH of the leachant. This study shows that most of the major elements captured in the ash residues could be mobilized when in contact with aqueous solutions of various pH. This reveals that the co-disposal of fly ash and brine may not be the best practice as the major elements captured in the ash residues could leach over time.  相似文献   

5.
In the present study, coal from Chakwal (Pakistan) was leached with an aqueous solutions of iodine monochloride (ICl) and diethylenetriamine pentaacetic acid (DPTA) of different concentrations. The effect of stirring time, concentration and pH was studied on the leaching of different metals from coal. The physicochemical parameters indicated that the coal was of reasonably good quality. The results indicated that with increase in time duration, the extraction of metals increased. In most of the cases, metal concentration increased in the leachate with increasing the concentration of the leaching agents. DPTA was found to be the best leaching agent for most of the metals. Higher extraction of metals from coal fly ash indicated that coal organic matter has a pronounced effect on the leaching. Higher concentration of metals was extracted from virgin coal and coal fly ash at low pH (p?>?0.00) as compared to high pH. DPTA extracted metals in higher concentration from virgin coal and coal fly ash at low pH as compared to ICl. Based on the present study, the most leached metals were Fe, Cu, Mn and the least were Pb, Ni, Cd and Cr.  相似文献   

6.
The leaching behaviour of fly ash from a Co smelter situated in the Zambian Copperbelt was studied as a function of pH (5–12) using the pH-static leaching test (CEN/TS 14997). Various experimental time intervals (48 h and 168 h) were evaluated. The leaching results were combined with the ORCHESTRA modelling framework and a detailed mineralogical investigation was performed on the original FA and leached solid residues. The largest amounts of Co, Cu, Pb and Zn were leached at pH 5, generally with the lowest concentrations between pH 9 and 11 and slightly increased concentrations at pH 12. For most elements, the released concentrations were very similar after 48 h and 168 h, indicating near-equilibrium conditions in the system. Calcite, clinopyroxenes, quartz and amorphous phases predominated in the fly ash. Various metallic sulfides, alloys and the presence of Cu, Co and Zn in silicates and glass were detected using SEM/EDS and/or TEM/EDS. The leaching of metals was mainly attributed to the dissolution of metallic particles. Partial dissolution of silicate and glass fractions was assumed to significantly influence the release of Ca, Mg, Fe, K, Al and Si as well as Cu, Co and Zn. The formation of illite was suggested by the ORCHESTRA modelling to be one of the main solubility-controlling phases for major elements, whereas Co and Zn were controlled by CoO and zincite, respectively. Sorption of metals on hydrous ferric oxides was assumed to be an important attenuation mechanism, especially for the release of Pb and Cu. However, there is a high risk of Co, Cu, Pb and Zn mobility in the acidic soils around the smelter facility. Therefore, potential local options for “stabilisation” of the fly ash were evaluated on the basis of the modelling results using the PHREEQC code.  相似文献   

7.
The mobility of inorganic pollutants is of key concern for a range of industrial and engineering applications of fly ash produced during the combustion of lignite in power generation. This paper investigates the role that the geochemical features of lignite, the ash composition and the partitioning of elements during combustion play in determining leaching properties of lignite fired by-products. The work is based on surveys on three lignite-fired power plants in Greece. Calcium-rich ashes show a high abatement potential for SO2 and other gaseous pollutants. For most elements, the concentrations in the parent lignite and the ashes follow the same trend. Relative enrichments in Cd, Co, Cr, Cu, Mo, Ni, Pb, U, V, W, Zn fingerprint the regional and local geological settings of the lignite basins. The total and leachable concentrations of highly volatile elements are strongly influenced by the interaction with ubiquitous free lime. A broad array of elements is highly insoluble in alkaline ash, while a few oxyanionic-forming elements display substantial mobility. Their mode of occurrence in the parent lignite plays a primary role in the leaching of combustion ashes. The outcomes of this study may assist in addressing the impact of co-firing high ash or high Ca alternative fuels on the leaching properties of combustion by-products.  相似文献   

8.
The phase–mineral and chemical composition of feed coals (FCs) and their bottom ashes (BAs) and fly ashes (FAs) produced in the Soma thermo-electric power station (TPS), Turkey, was characterized. FCs are high-ash Soma subbituminous coals abundant in moisture and Ca, and depleted in S. The inorganic composition (in decreasing order of significance) of FCs includes calcite, quartz, kaolinite, illite+muscovite, chlorite, plagioclase, gypsum, pyrite, montmorillonite, K-feldspar, dolomite, siderite, ankerite, opal, and volcanic glass. The results for 57 elements studied show that Ca>Nb>Cs>(V, Li) have significantly higher contents in FC ashes than the respective Clarke values for coal ashes. The water-soluble residues isolated from FCs include gypsum, calcite, inorganic amorphous matter, Ca–Mg–Na–K phase, and opal. These residues are enriched in Na>Se>S>B>Mg>Mo>Sr>Ca>K. The phase–mineral composition of BAs and FAs includes mainly glass, quartz, char, mullite, plagioclase, calcite, and portlandite; and, to a lesser extent, illite+muscovite, melilite, hematite, anhydrite, lime, cristobalite, kaolinite, and magnetite. Minor amounts of K-feldspar, dolomite, ankerite, Fe-spinel, gypsum, and Ca–K–Na phase also occur in BAs and FAs. FAs are enriched in inorganic matter, glass, cristobalite, mullite, Fe oxides, lime, and anhydrite, and depleted in mineral matter, char, quartz, clay minerals, melilite, portlandite, and carbonates in comparison with BAs. Only Se is significantly enriched in BAs and FAs compared to FC ashes. Most of the trace elements (in particular As, Bi, Cd, Ge, Pb, Sn, Tl, and W) are more abundant in FAs, while BAs are more enriched in Ca, Cs, Fe, Ho, Mn, P, Sc, Se and Tb. Significant percentages (11–59%) of elements initially present in FCs, namely S>Sb>Sn>Ta>Mo>Bi>Zn>Ni>Na>(Lu, Tm)>B, were emitted by stack emissions and not captured by the cleaning equipment in the Soma TPS. Some genetic features, properties, possible environmental concerns, and potential utilization directions related to FCs, BAs, and FAs are also discussed.  相似文献   

9.
Abstract. Municipal solid waste combustion leads to concentration of various metals in the solid residue (fly ash) remaining after combustion. These metals pose serious environmental hazard and require proper handling and monitoring in order to control their harmful effects. Leachability of some metals from fly ash was examined in fly ash and Milli-Q water mixture (liquid-to-solid ratio, 100) under various temperature and pH conditions in the laboratory. The leaching experiments conducted for 24 hours showed that pH was generally more important than temperature in controlling the amount of metals leached out of the fly ash. However, at a given pH, rise in temperature led to different degree of (usually one to two fold) enhanced or reduced leaching of metals. Owing to amphoteric nature of oxides of Al, Cr, Pb and Zn, these metals often yielded typical pattern of increase and decrease in their concentrations with change in pH. The extent of leaching of Cr and Pb in our experiments suggests that decrease of pH to acidic range in the case of Pb and to neutral to acidic range for Cr over a long period of storage of fly ash at solid waste dumping site may facilitate leaching of these metals from fly ash, leading to contamination of groundwater to the level that exceeds beyond the level permitted by the environmental laws.  相似文献   

10.
Abstract. Oxidation and reduction processes can influence extent of leaching of elements from solid waste. Three samples of municipal solid waste combustion fly ash were subjected to oxidizing and reducing conditions in order to evaluate leaching of elements in the Milli-Q water and fly ash (liquid to solid ratio, 100) mixtures. Although the oxidizing and reducing conditions were applied for 6 hours only, elements like Cs, Li, Mg, Sb, Tl and V leached more under oxidizing condition than under reducing condition in the case of all three ash samples. Cadmium, Pb and Zn leached more from all samples under reducing condition than under oxidizing condition. Leaching of other elements like Al, Ba, Cr, Cu, Ni and Rb was inconsistent with oxidizing or reducing conditions and varied from sample to sample, suggesting that factors other than redox may be more important in controlling leaching of these elements. Strong acid neutralization capacity of the fly ash samples let the pH vary within a narrow range, and thus severely limited the extent of leaching during the course of the experiment. Lead and Zn were the most sensitive while K and Na were the least sensitive to changes in redox conditions.  相似文献   

11.
Combustion of coals in thermal power plants is one of the major sources of environmental pollution due to generation of huge amounts of ashes, which are disposed off in large ponds in the vicinity of the thermal power plants. This problem is of particular significance in India, which utilizes coals of very high ash content (∼55 wt%). Since the thermal power plants and the ash ponds are located in densely populated areas, there is potential chance for contamination of soil and groundwater of the surrounding areas from the toxic trace elements in the ash. An attempt has been made to study the extent of soil contamination around one of the largest thermal power plants of India located at Kolaghat, West Bengal India. Chemical analysis of the top soils and the soils collected from the different depth profiles surrounding the ash ponds, show that the top soils are enriched in the trace elements Mo, As, Cr, Mn, Cu, Ni, Co, Pb, Be, V, Zn, which show maximum enrichment (2–5) in the top soils collected from all the soil profiles. These elements are also enriched in the pond ash. Since there are no other sources of industrial effluents, it can be said that the enrichment of the trace elements (Mn, Co, Mo, Cr, Cu, Pb, Zn, As, Ni, Be, V) is attributed to their input from ash from the disposal pond. The study has been further strengthened by log-normal distribution pattern of the elements.  相似文献   

12.
A new method of simultaneous multi-elemental analysis, Proton Induced X-ray Emission (PIXE), was used to detect trace elements in waters associated with a coal strip-mining operation in southern Indiana. Stream, pond, and ground water samples were collected and analyzed monthly from, or near, Sulphur Creek in Sullivan County. The concentrations of 26 major and trace elements were determined in samples from eleven locations: K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Br, Rb, Sr, Mo, Cd, Sn, Sb, I, Ba, Hg, Pb, and U. Elemental concentrations fluctuated considerably throughout the 13-month sampling period and also among sampling sites. Nickel, Zn, As, Cd, Mn, Fe, and Ca were highest in the upstream water which was most acidic (pH = 2.9–4.0) because of old unreclaimed mining operations. The highest values recorded were Ni = 1662 ppb, Zn = 4953 ppb, As = 26 ppb, Cd = 93 ppb, Mn = 5063 ppb, Fe = 63 ppm, and Ca = 325 ppm. The concentrations of these elements decreased downstream as the pH of Sulphur Creek increased which was likely due to the influence of the calcareous glacial till cover in the area and the recent mining activity which disturbed overburden containing a high percentage of calcareous materials. Lead, I, Br, and Ti values were highest (661 ppb, 86 ppb, 70 ppb, and 45 ppb, respectively) in the ground water from the coal seam (pH approximately 7). Other elements which were relatively high in the pH 7 waters closest to the current mining operations (pond, stream, and groundwater) included K (17 ppm), Sr (3408 ppb), Ba (173 ppb), As (14 ppb), Rb (16 ppb), Sn (14 ppb), and Cu (3840 ppb). The highest Cu concentration was recorded at the point where drainage water from the mine entered Sulphur Creek. Gallium, U, Hg, and Mo were found in low (< 13 ppb for Ga and Hg; < 205 ppb for Mo and U) concentrations and only in the ponds within the mine.  相似文献   

13.
Geochemical responses in weathered and oxidized surface metasedimentary rocks associated with stratiform lead-zinc mineralization at Stirling Hill (6 km west of Broken Hill) are compared with the geochemical responses in fresh drill core from an equivalent lithostratigraphic section with stratiform lead-zinc mineralization at the Pinnacles Mine (8 km south of Stirling Hill). Mineralization is interpreted as being volcanic exhalative and it lies within highly metamorphosed (sillimanite grade) rocks of the Willyama Supergroup.Surface rocks were classified into groups by discriminant analysis using drill core data from the Pinnacles Mine as the initial training set. The behaviour of elements in surface rocks varies with the rock group but Zn, Pb, Mn, Fe, and Co are leached from all surface rocks relative to fresh drill core.Nothwithstanding the leaching effects of weathering, common geochemical responses to mineralization have been identified in drill core and surface rocks. Coincident positive anomalies for Zn/Ba and Fe/(Na × Ba) ratios and negative anomalies for Na/(Mn × Ca) ratios uniquely define mineralization in both weathered surface rocks and in fresh drill core.The results demonstrate that the pattern of geochemical responses to Pinnacles-type stratiform volcanic-exhalative mineralization in surface rocks has survived the intensive weathering regime in the Broken Hill region.  相似文献   

14.
 In 1995, the central heating plant Draken in Kalmar, Sweden, started manufacturing a granular ash product for nutrient recycling to forest soil, instead of dumping the ash in landfills. Chemical composition, leaching and dissolution characteristics were determined for the Draken wood ash, the dolomite used in granule manufacturing and the final granule product. The heavy metal concentrations in fly ash were within the limit values recommended by the Swedish National Board of Forestry for ash recycling, except for Cd and As levels which occasionally exceeded the limit values. The Ca, Mn and P levels were too low for nutrient recycling at the time. Adding dolomite insures that the levels of the important nutrients Ca and Mg are sufficient in the granules. After 7 months in the field, about 60 % of Na and K was leached out from granules. Between 20 and 60% of trace elements Mo, Sc, V, Y and Zr were leached out after 7 months. The release of Ca and Mg was low, 1–5% during 7 months. Received: 12 July 1999 · Accepted: 31 August 1999  相似文献   

15.
The bulk of fly ash (an inorganic waste of coal-fired power generation) produced is deposited in disposal areas where it needs to be revegetated. The effects of addition of three conventional organic amendments (biosolids, poultry manure, green waste compost), or poultry manure-derived biochar, to coal fly ash (at two rates) on some key chemical, physical and microbial properties and on growth of Rhodes grass (Chloris gayana) was studied in a laboratory incubation/greenhouse study. Addition of all amendments, including biochar, increased concentrations of extractable Mg, K, Na and P and CEC(pH 7.0). Additions of poultry manure, and particularly biosolids, also greatly increased levels of extractable NH4 + and NO3 −-N. Addition of biosolids, green waste compost and biochar resulted in a decrease in macroporosity, a concomitant increase in mesoporosity and, at the high rate of addition, an increase in available water-holding capacity. Basal respiration was very low in fly ash and was increased by addition of all amendments; metabolic quotient was markedly greater in control than amended treatments. Biosolids, poultry manure and green waste compost additions all increased microbial biomass C. Growth of Rhodes grass was extremely low under unfertilized conditions in control, biochar and, to a lesser extent, green waste compost treatments but addition of poultry manure and the lower rate of biosolids resulted in large increases in yields. Although biochar additions increased extractable Ca, K, P, Cu, Zn and Mn, CEC, mesoporosity and water-holding capacity, they had a little or no stimulatory effect on the size of the soil microbial community, N fertility or plant growth. This was attributable to the lack of metabolisable C and an insignificant N-supplying capacity.  相似文献   

16.
The results of a surface rock chip sampling study over a small distal volcanogenic massive sulphide deposit at Limerick, N.S.W., Australia are presented and compared with drill core and soil geochemical patterns. Major element halos are narrow in comparison to the pervasive patterns reported from major proximal deposits. Narrow zones of Mg and K enhancement are associated with sulphide mineralization. High levels of Na occur in these rocks in contrast to the regularly described pattern of Na depletion. Weathering, particularly in the presence of sulphides, has resulted in the leaching of Ca, Na and, to a lesser extent, K from surface rock chip samples, whereas Fe, Pb and Zn contents are enhanced compared to those in fresh rocks. Despite the problems of sample heterogeneity, variable weathering and the limited extent of alteration halos which exist in this environment, surface lithogeochemical methods in comparable situations may be useful in the confirmation and interpretation of soil geochemical anomalies.  相似文献   

17.
In order to investigate the factors influencing the distribution of 32 potentially toxic elements in the Ptolemais–Kozani basin, northwestern Greece, 38 soil samples were collected and analyzed. Concentrations of Al, Ca, Fe, K, Mg, Mn, Na, P, Ti, Ba, Co, Cr, Cu, La, Li, Ni, Pb, Sc, Sr, V, Y, and Zn were determined by ICP-AES and concentrations of As, Bi, Cd, Cs, Mo, Rb, Sb, Th, Tl, and U by ICP-MS. Bivariate analysis, principal component analysis, and geostatistical analysis were employed to investigate the factors influencing the distribution of the elements determined in the study area. The results indicate that the distribution of the majority of elements determined, especially for Cr, Ni, and associated elements, is greatly influenced by the geology and geomorphology of the study area. Principal component analysis has yielded four factors that explain over 77% of the total variance in the data. These factors are as follows: lithophilic elements that are associated with Al silicates minerals of K (factor I: 29.4%), ultramafic rocks (factor II: 20.5%), elements that are coprecipitated with Fe and Mn oxides (factor III: 18.0%), and anthropogenic activities (factor IV: 9.3%). The anthropogenic activities that influence the distribution of several potentially toxic elements (i.e., Cd, Cu, Pb, Zn) are agricultural practices and the deposition of fly ash in the vicinity of the local power stations.  相似文献   

18.
Fly ash is a waste by-product obtained from the burning of coal by thermal power plants for generating electricity. When bulk quantities are involved, in order to arrest the fugitive dust, it is stored wet rather than dry. Fly ash contains trace concentrations of heavy metals and other substances in sufficient quantities to be able to leach out over a period of time. In this study an attempt was made to study the leachabilities of a few selected trace metals: Cd, Cu, Cr, Mn, Pb and Zn from two different types of class F fly ashes. Emphasis is also laid on developing an alternative in order to arrest the relative leachabilities of heavy metals after amending them with suitable additives. A standard laboratory leaching test for combustion residues has been employed to study the leachabilities of these trace elements as a function of liquid to solid ratio and pH. The leachability tests were conducted on powdered fly ash samples before and after amending them suitably with the matrices lime and gypsum; they were compacted to their respective proctor densities and cured for periods of 28 and 180 days. A marked reduction in the relative leachabilities of the trace elements was observed to be present at the end of 28 days. These relative leachability values further reduced marginally when tests were performed at the end of 180 days.  相似文献   

19.
The maximum concentration of the majority of the trace metals in the leachates from shake and column test of lignite fly ash (LFA) was within the prescribed limits; however, total dissolved solids, total hardness, cations and anions (except K+), being above the prescribed limits, may lead to the increase in the hardness and salinity in the soil on the disposal of LFA. Present generation of huge amount of fly ash from thermal power plants (TPPs) is a big challenge concerning contamination of soil, crop produce and surface and ground water bodies due to the presence of some of the toxic trace metals in it. The leaching behavior of alkaline LFA (pH, 10.94), from TPP of Neyveli Lignite Corporation (NLC), India, was investigated by shake and column tests using water and sodium acetate buffer. The leaching of trace metals from LFA was governed by their concentrations, association with the ash particles, leaching duration and pH of the leachate (most influencing parameter). The leaching of metals followed the order: buffer column > aqueous column > aqueous shake > buffer shake test.  相似文献   

20.
This study is focused on the occurrence and distribution of mineral matter and major and trace elements in the high volatile bituminous coal from Puertollano (south-central Spain). The relationship between ash behaviour and inorganic composition, as well as the possible formation of fouling and slagging deposits in boilers during the conversion process, were investigated. The Puertollano coals do not exhibit plastic properties, despite their rank, probably because of their high ash and inertinite contents.The Puertollano coal has medium to low total S content (0.48% to 1.63% db, with a mean of 1.0% db) and is characterised by relatively high contents of Si, Pb, Sb, and Cs. Some elements such as As, Cd, Co, Cr, Cu, Ge, Li, Mn, Ni, W, and Zn are also present in relatively high contents. The enrichment in a number of heavy metals could be attributed to the common sulphide ores occurring near the Puertollano coal deposit.The following trace elements affinities are deduced: (a) sulphide affinity: As, Co, Cd, Cu, Ni, Sb, Tl, and Zn; (b) aluminum–silicate affinity: K, Ti, B, Co, Cr, Cs, Cu Ga, Hf, Li, Nb, Rb, Sn, Ta, Th, V, Zr, and LREE; (c) Carbonate affinity: Ca, Mg, Mn, and B; (d) organic affinity: B.The very high Si levels and the anomalous enrichment in Cs, Ge, Pb, Sb, and Zn shown by the Puertollano coals account for the high contents of these elements in the Puertollano fly ash when compared with the other Spanish coal fly ashes.The chemical composition of the high temperature ash (HTA) is consistent with the trend shown by the ash fusion temperatures (AFT) and also with the predictive indices related to slagging and fouling propensities. Thus, the ash fusion temperatures increase with high values of Al2O3 as well as with the decrease in Fe2O3, CaO, and MgO.  相似文献   

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