an assessment of soil contamination due to heavy metals around a coal-fired thermal power plant in...
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Environmental Geology
International Journal of Geosciences
© Springer-Verlag 200610.1007/s00254-006-0336-8
Original Article
An assessment of soil contamination due to
heavy metals around a coal-fired thermal
power plant in India
A. Mandal 1 and D. Sengupta 2
Planetary and Geosciences Division, Physical Research Laboratory, Navrangpura, Ahmedabad, 380009,India
Department of Geology and Geophysics, IIT Kharagpur, Kharagpur, 721302, India
A. MandalEmail: [email protected]
D. Sengupta (Corresponding author)Email: [email protected]
Received: 2 April 2006
Accepted: 4 May 2006
Published online: 26 July 2006
Abstract
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 andFirefox can't load web fonts from a remote host
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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.
Keywords Fly ash – Bottom ash – Trace elements – Enrichment factor –Log-normal distribution
Introduction
The global energy needs have enormously increased with rapid strides in
technology and, these have been met, to a large extent from fossil fuels.
Coal-fired power plants generate about 23% of the electricity consumed
worldwide (EIA 2002). One of the major environmental problems associated
with the use of coal as fuel in thermal power plants is the production of ash.
This problem is particularly important for Indian power stations because most
of the power stations use poor quality coal with 5–50% ash yielding about
100 million tons of ash per annum (Vijayan and Behera 1999). The solid wastes
produced from the coal-fired thermal power plants are mainly of two types, i.e.
fly ash and bottom ash. Bottom ash is the coarse-grained fraction that is
collected from the bottom of the boiler and is disposed of by the wet disposal
method in a slurry form to nearby waste disposal sites (ash ponds). Fly ash
consists of finer sized particles, ranging from 0.5 to 200 μm (Baba 2002).
Owing to its relatively small size and, hence, large surface area, the ashes
have a greater tendency to absorb trace elements that are transferred from
coal to waste products during combustion (Gulec et al. 2001). Migration of the
trace elements from waste disposal sites to surrounding ecosystems is a
complex process. Trace elements present on the surface of ash particles are
readily leached (Shi and Sengupta 1995; Fytianos et al. 1998) and tend to
contaminate the groundwater (Theis and Gardner 1990; Theis et al. 1978;
Carlson and Adriano 1993).Firefox can't load web fonts from a remote host
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Soil is a mixture of natural bodies on the earth surface containing living
matter and supporting plants (Russal 1957). Soil is complex substance
because of its variation in physical and chemical composition. It contains small
significant quantities of organic and inorganic compounds, which are essential
for the growth of plants.
Soil contamination by heavy metals from waste disposal sites is a serious
problem in industrial and urban areas. Soil is the ultimate and most important
sink of trace elements in the terrestrial environment. Heavy metals are mainly
introduced to the environment through anthropogenic activities such as those
related to metal mining, metallurgical processing and waste disposal. Metal
contamination of surface soils (Pichtel et al. 1997), agricultural soils (Kim and
Kim 1998; Sharma et al. 2000), from industries (Ullrich et al. 1999; Bityukova
et al. 2000; Sterckeman et al. 2000) and waste disposal sites (Yarlagadda et al.
1995) is well known. Soil contamination around coal ash disposal sites takes
place in two different ways: through atmospheric fallout and due to leaching.
The topsoil (0–15 cm from the surface) is mainly affected by the ash fallout.
Atmospheric deposition from industrial activities can induce long-term
changes in soil quality (Jones 1991). Bertine and Goldberg (1971) have shown
that fossil fuel combustion can be a potentially significant source of
atmospheric discharge of many metals. Heavy metals from fossil fuel
combustion are a common source of pollution for surface soils (Parekh and
Husain 1987; Ramachandran et al. 1990). The inhomogeneties in the soil
composition may exert significant influences on individual and distribution
characteristics (Kim and Kim 1998). Contamination of surrounding soil due to
the deposition of air-borne ash plume from the disposal pond (Satyanarayana
Raju 1993; Praharaj et al. 2001) has been a matter of great concern.
Continuous input of ash into the soil has the potential to affect the
physicochemical characteristics of the soil (Carlson and Adriano 1993; Bilski
et al. 1995). Most trace elements act as micro-nutrients to certain plants but
become toxic at enhanced levels in the soil, thereby contaminating the land
(Mukherjee and Nag 1997). Coal ash contains high concentration of trace
elements, which affect the soil properties and vegetation grown around the
ash disposal site. Studies by Bityukova et al. 2000 on the pollution of soil
around industries have shown that the levels of As, Cr, Mn and V were more
than three times higher and levels of Pb and Zn were more than five times
higher than the background levels.
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Coal combustion from thermal power plants contributes to 86% of the total
electricity generation in Eastern India as compared to the other parts of India.
The Kolaghat thermal power plant, in West Bengal, in Eastern India is the
second largest, next to Farakka. Nearly 14,000 tonnes of coal are burnt to run
the six units of the Kolaghat Thermal Power Plant, emitting 5,000 tonnes of
ash. But there are only four ash ponds, covering an area of 253 acres, which
do not have the capacity to accommodated such huge quantities of ash.
Kolaghat officials feel that at least 1,253 acres of land are required for
depositing the ash. The ash is deposited both by the dry and wet disposal
methods. In the dry method, the ash is transported in trucks and dumped in
open ponds located 3 km S, SW and NW of the power plant, near the villages
of Rakshachak, Bahala and Mecheda. Absence of covering of the ash pile in
the trucks causes it to fly in the prevalent wind direction. Apart from this the
ash is also mixed with water to form slurry and then transported through
pipes to disposal ponds, where upon disposal it gets dried by the sun, becomes
hard and compact and constitute the top soil of the region. Due to
unavailability of enough open unused lands, agricultural lands on which the
locals rely for their food needs are also filled up with the ash. Geochemical
studies carried out by Mandal and Sengupta (2005) have shown that the ashes
of Kolaghat contain sufficient amounts of trace elements As, Cu, Pb, Ni, Zn,
Co, V, Sc, Be, Cs and Zr relative to the feed coal. These elements show
significant enrichment in the pond ash relative to their crustal abundance.
Trace elements present in the ash may get incorporated in the top soil from
the wind blown ash particles and also from the ash dumped, since there are no
underground lining beneath the ash pile dumped. Hence in the present study
it was thought pertinent to study the characterize the soil in terms of
mineralogy and geochemistry especially on the basis of heavy metal
concentration as excess concentration of trace elements in the soil is harmful
for the growth of the plants, which will indirectly effect the agriculture of the
region.
The enrichment of individual elements in the top soil around the ash pond was
estimated with respect to the crustal abundance and also with respect to the
background to show the effect of ash deposition on the soil.
Study area
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The present study was conducted around the ash disposal sites of the Kolaghat
thermal power plant, situated in the Midnapur district of West Bengal, India.
The area under study falls under the Survey of India toposheet No. 73N/15
and is bounded by north latitudes 22°25′ and 22°27′ and east latitudes 87°50′
and 87°55′. The thermal power plant consumes bituminous coal of grade E and
F. It has six units of 210 MW each and generates 1,260 MWe electricity.
The Kolaghat region falls within the Kasai delta of the Upper Holocene Dainkri
formation with dominant lithotypes being laterites with brown and mottled
clays at the top. The major source of potable water for the villages Raksha,
Bahala and Mecheda surrounding the ash pond are the Kasai river, the Denan-
Dehati canal and the tributaries of the Rupnarayan river (Fig. 1a). Earlier, the
fly ash generated was collected from the electrostatic precipitators, but now
both the bottom ash and the fly ash (from the electrostatic precipitators) of the
plant are mixed together and deposited in dry and wet disposal method in the
four large ponds (1A, 1B, 4A, 4B) (Fig. 1b) located 4 km south, south–west and
north–west of the power plant. Ash ponds 1A and 1B are located west and
north–west of the power station and on either side of National Highway NH-6,
whereas the ash ponds 4A and 4B lie to the south of the power plant, on either
side of the railway track. The adjacent areas of ash pond continuously receive
atmospheric fallout and wind blown ash particles from the pond.
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Fig. 1
a Location map of the study area. b Location of the sites from where soil samples were collected
Methodology
Sample collection
Topsoil (0–5 cm) samples were collected around the ash ponds from four radial
profiles, 1A1–1A4, 1B1–1B4,4A1–4A4, 4B1–4B4, in each of the ash ponds.
Samples were collected from each profile at regular intervals of 10 m. Besides
the topsoil, soil samples were also colleted from two vertical profiles (D1and
D2) at depths of 0, 25, 50 and 100 cm from the surface. Background soil
samples were collected at distance of about 10 km south of the ash ponds
(Fig. 1b). The background samples are selected from areas which are not
affected by fly ash disposal, i.e. these are the areas where the ash from the
ponds is not dumped by either wet or dry disposal methods. As stated earlier
the ash are dumped 3 km near the power plant, so at 10 km distance the soil is
almost unaffected by ash pile.
Laboratory methods
The soil samples were homogenized by coning and quartering, air-dried at
100–110°C for about 24 h and then finely powdered and sieved using standard
sieves of (70, 100, 140, 200, 270, 325) mesh size before analysing for trace
element concentration using an X-ray fluorescence spectrometer, Philips 1450
and automatic sequential (wavelength) spectrometer equipped with a
Ph-target X-ray tube at IIT Kharagpur. The tube was operated at 45 and
60 kV/50 mA and 60 kV/40 mA for optimum excitation of the analytes.
X-ray diffraction (XRD) analysis of soil and sediments was carried out for
mineral phase identification by Phillips diffractometer (PW 1840) coupled with
X-ray generator (PW 1729), using Cu-Ka. All the samples were run at a tube
voltage of 20 kV and 30 mA. The goniometer speed and chart speed were
maintained at 0.05 2 h and 10 mm/2 h, respectively.
The pH was measured at a solid to liquid ratio of 2:5 using an Orion 1260 Ion
Selective Electrode (ISE). The trace elements in soil samples were determinedFirefox can't load web fonts from a remote host
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by using the inductively coupled plasma-mass spectroscopy (ICP-MS), MODEL
Perkin Elmer Sciex ELAN DRC II (Toronto, Canada) at the Central Research
Facility available at National Geophysical Research Institute, Hyderabad,
India. Solutions of the soil samples were prepared by the microwave
dissolution technique. A microwave digestion system, Model MARS-5 (CEM
Corporation, Matthews, NC, USA), equipped with 12 low-volume
perfluoroalkoxy (PFA) lined vessels, with safety rupture membranes (maximum
operating pressure 1,380 Kpa), was used for microwave dissolution. A rhodium
solution of 1 mg/l concentration was added as 10% v/v as an internal standard
(Balaram 1993). International soil reference materials were used to prepare
calibration curves for different trace metals and to check the accuracy of the
analytical data. Canadian soil reference materials SO-1, SO-2, SO-3 and SO-4
were used to estimate the analytical bias of the soil data. The detection limits
for all the trace elements were better than 1 ng/ml (Govil et al. 1997). The
precisions obtained for most of the trace elements data was <5% RSD with
comparable accuracy (Balaram 1993).
Results and discussions
Mineralogy
Size analysis of the samples show that majority of the soil samples were in the
range of 149–105 μm and <53 μm. Size classification shows that the soils upto
100 cm depth in all the profile as well as the top soils are of fine sand to silt to
clay range. The X-ray diffractogram of the bulk soils samples from the profiles
around the ash ponds are shown in Fig. 2a, b. It is seen that the major
mineralogical phases identified in the soil were kaolinite, illite, mullite and
quartz. The diffractograms of the samples from 4A, 4B, indicated the presence
of mullite (3Al2O3·2SiO2) as one of the major mineralogical phases. The
presence of mullite in the X-ray diffractograms of the topsoil from profiles 4A,
4B is a striking observation. Mullite, a common mineral in coal ash, is
normally not found in natural soils (Lumsdon et al. 2001). Mullite is also
present in the X-ray diffractograms of the ash samples of the study area
(Mandal and Sengupta 2002, Fig. 3). Hence its presence in the top soil could
be attributed mainly to the contribution either from the wind blown ash
particles or from the ash dumped.Firefox can't load web fonts from a remote host
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Fig. 2
X-ray diffractogram of top soil around ash pond 4A and 4B
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Fig. 3
XRD pattern of pond ash from the ash ponds of Kolaghat
Chemical composition of the top soils from the four soil profiles
The pH of the soil was in the acidic range 4.5–5.2 in all the soil samples
studied. The pH of ash deposited was also acidic in nature ie 4.5. The pH of
the background soil was alkaline (8.2), which showed that the acidic nature of
the pH of the soils near the ash ponds was due to the effect of ash disposal.
The top soils of all the soil profiles from all the ash ponds are characterized by
dominance of SiO2 followed by Al2O3, Fe2O3, K2O and TiO2 as seen in Table 1.
The trace elements analysed in the profile soils around the four ash ponds and
the background soils are shown in Table 2. The trace elements in decreasing
order of abundance in all the soil profiles around the four ash ponds are Mn,
Ba, Rb, Sr, V, Zn, Cr, Ni, Cu, Pb, Mo, Be and As. It is observed that the element
concentrations are varying from profile to profile around the ash pond while
their variations within the same profile did not show any particular trend.
Among the trace elements Mn, Ba, V, Cr, Cu, Zn Pb showed much higher
concentrations in the top soils from all the profiles around the four ash ponds
than the background soils.
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Table 1
Major and minor oxides (wt%) in the top soils from the soil profiles around the four ash ponds (1A, 1B, 4Aand 4B)
SiO2 Al2O3 TiO2 Fe2O3 CaO MgO K2O P2O5
1B1 62.11 10.01 1.79 4.50 2.03 1.30 2.89 0.29
1B2 63.10 11.02 1.52 4.67 2.21 1.32 2.92 0.28
1B3 64.10 12.12 1.67 4.56 2.12 1.29 2.95 0.27
1B4 62.21 10.32 1.56 4.64 2.03 1.19 2.98 0.29
Average 62.88 10.87 1.64 4.59 2.10 1.28 2.94 0.28
1A1 62.11 12.22 1.32 4.23 2.32 1.23 2.12 0.32
1A2 64.10 12.32 1.54 3.67 2..30 1.29 2.23 0.29
1A3 63.10 13.21 1.45 3.98 2.39 1.28 2.34 0.3
1A4 62.21 11.09 1.53 4.1 2.56 1.31 2.29 0.31
Average 62.88 12.21 1.46 4.00 2.42 1.28 2.25 0.31
4A1 62.11 11.01 1.89 4.56 2.12 1.45 2.89 0.29
4A2 64.10 12.30 1.72 4.67 2.34 1.42 2.92 0.28
4A3 69.11 12.12 1.67 4.63 2.45 1.38 2.95 0.27
4A4 72.10 10.32 1.56 4.64 2.56 1.41 2.98 0.29
Average 66.80 11.44 1.71 4.62 2.37 1.42 2.94 0.28
4B1 66.11 12.22 1.32 4.23 2.45 1.32 2.12 0.32
4B2 64.11 12.32 1.54 3.67 2.65 1.39 2.23 0.29
4B3 68.10 13.21 1.45 3.98 2.78 1.54 2.34 0.3
4B5 62.21 11.09 1.53 4.10 2.56 1.52 2.29 0.31Firefox can't load web fonts from a remote host
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Table 2
Trace elements in the top soils from the four profiles around the four ash ponds (1A, 1B, 4A and 4B) and thebackground soil (BG) (all values in ppm)
Sampleno.
Trace elements
Be V Cr Mn Ni Co Cu Zn
1B1 4.36 127.00 97.40 1260.00 71.63 20.29 84.05 210.30
1B2 4.31 135.00 123.41 1265.00 62.19 21.50 89.74 218.02
1B3 4.33 140.00 70.40 1264.00 37.22 13.97 66.15 164.89
1B4 4.35 145.00 122.54 1261.00 49.14 20.67 54.15 185.35
Average 4.34 136.75 103.44 1262.50 55.05 19.11 73.52 169.64
1A1 4.33 125.84 95.75 1208.00 45.92 17.86 57.87 99.82
1A2 3.85 115.49 73.73 1250.00 40.73 14.16 57.87 137.36
1A3 4.31 115.61 96.29 1210.00 45.87 19.42 59.00 91.87
1A4 4.18 137.03 102.61 1220.00 56.05 19.28 59.38 183.25
Average 4.17 123.49 92.09 1222.00 47.14 17.68 58.53 128.08
4A1 5.63 155.00 105.40 1500.00 76.63 27.86 84.05 219.30
4A2 5.44 152.00 131.41 1529.00 67.19 24.16 89.74 227.02
4A3 4.82 150.00 78.40 1520.00 42.22 29.42 86.15 173.89
4A4 5.43 158.00 130.54 1521.00 54.14 31.10 84.15 94.35
Average 5.33 153.75 111.44 1517.50 60.05 28.13 86.02 178.64
4B1 5.33 142.00 121.00 1390.00 45.92 20.29 77.87 79.82
4B2 4.85 143.00 73.73 1500.00 40.73 21.50 59.00 70.82
4B3 5.31 134.00 96.29 1520.00 45.87 23.00 56.72 137.36Firefox can't load web fonts from a remote host
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Trace elements in the depth profiles
The concentrations of trace elements in soils collected with depth (e.g., 0, 25,
50, 75 and 100 cm) from two profiles (D1) and (D2) are shown in Table 3,
Fig. 4a, b. It is seen in that in all the depth profiles (D1 and D2), the
concentration of the trace elements decreases with depth. The concentration
of the trace elements Mn, Ba, V, Cr, Cu, Zn, As decreases below the surface
layer, i.e. from 0 to 25 cm. It is significant to note that all these elements are
abundantly present in the coal ash and are enriched 2–10 times with respect
to their crustal abundances (Table 4). The pond ash, which is mixed with the
top soil layer in all the ash ponds, is characterized by high concentrations of
toxic trace elements (As, Cd, Cr, Ni, Co, Cu, Sb, V, Zn, Mn, Mo) (Mandal and
Sengupta 2002). Therefore, it may be inferred that the topsoil, with high
concentration of trace elements in both the depth profiles, is possibly
contaminated by ash from the pond. Since there are no other industrial
emissions in the study area, the high concentrations of the trace elements in
the top soils implies input from the ash piles, which lie uncovered and exposed
to the atmosphere. Wind blown ash particles are easily carried away due to
their fineness and deposited as a layer on the top soils of the surrounding
areas.
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Table 3
Variation of element concentrations in the depth profiles D1 and D2 (all values in ppm)
Profiles D1 D2
Depth(cm)
0 25 50 75 100 0 25
Elements Concentration (ppm)
Be 4.34 3.75 2.90 2.78 1.66 5.33 2.78
V 132.02 127.20 112.32 97.91 90.05 153.75 140.37
Cr 107.58 103.44 94.35 83.71 79.71 111.44 104.23
Mn 1,262.50 1,032.21 921.92 897.63 873.34 1,321.00 1,201.00
Ni 55.05 45.47 41.92 34.35 27.78 71.08 66.05
Co 19.11 18.82 18.54 18.26 17.97 28.13 24.61
Cu 90.38 73.52 69.55 56.99 46.57 94.94 86.02
Zn 169.64 163.21 156.78 150.35 143.93 178.64 169.53
As 4.67 4.12 3.45 2.86 2.25 3.98 2.47
Rb 166.32 164.33 162.34 160.35 158.35 234.25 214.58
Sr 126.63 120.16 115.46 110.50 10.8.20 154.12 150.01
Mo 8.57 6.21 6.16 5.57 4.37 7.05 5.75
Ba 666.25 654.00 650.00 640.50 632.38 684.47 654.00
Pb 25.24 23.07 16.23 14.02 12.21 35.57 30.14
U 8.39 7.91 6.40 5.40 4.87 7.91 6.40
Th 28.63 25.29 24.70 21.12 20.12 22.01 2012.00
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Fig. 4
a Depth wise distribution of (Ba, Mn) in the two soil profiles D1 and D2. b Depth wise distribution of (Be, As,Mo, Ni, Co, Cr, Cu, Pb, V, Zn, Rb, Sr) in the two soil profiles D1 and D2
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Table 4
Concentration of trace elements and their enrichment factor is pond ash
Trace elements in pond ash Concentration (ppm) EF (ash)
Mn 5,459.19 10.28
Cr 135.1 4.32
Mo 13.16 9.81
Cd 0.91 10.43
Be 5.87 2.19
Sc 34.2 3.48
V 195.75 3.65
Co 33.33 3.71
Ni 60.11 3.36
Cu 86.71 3.88
Zn 119.53 1.88
As 10.03 7.01
Rb 253.87 2.53
Sr 269.26 0.86
Zr 822.84 4.84
Ba 1,052.2 2.14
Pb 94.75 5.30
Enrichment of elements
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(1)
(2)
The enrichment factors (EFs) for different elements in topsoil were calculated
with respect to their crustal abundance (Taylor and McLenan 1985) and
background concentration. The EF was calculated by using different formulae
as given below:
where (C i /C Si)soil = (Concentration of ‘i’/Concentration of Si) in soil, (C i /C
Si)Crust = (Concentration of ‘i’/Concentration of Si) in the crust, (C i /C Si)BG =
(Concentration of ‘i’/Concentration of Si) in the background soils.
For the calculation of EF with respect to the crust and the background, silicon
(Si) was used for normalization as it is known to be very stable in the
geochemical environment of the crust. The enrichment factors of the trace
elements with respect to the crust are shown in Table 5. With respect to the
crust, all the EF values were within the range of 0.4 to 5.8. The higher values
were for Mn (2.1–2.6), Mo (3.8–5.8), Cr (2.6–3.2), Cu (2.5–3.5), As(1.9–3.8),
V(2.1–2.6), Zn (1.8–2.5), Co (1.8–2.8) and Ni (2.4–3.0). Table 6 shows the
enrichment factors of the trace elements and the radionuclides with respect to
the background soils. With respect to the background soils, all the elements
showed EF values were within the range of 0.9–6.5. The higher values were
for Mn (2.1–2.7), Ba (4.5–4.9), V (5.3–6.5), Cu (4.1–5.6), Zn (3.4–5.2). The
enrichment of all the elements in the top soil attributed to their input from ash
from the disposal pond and by wind blown ash particles.
EF in soil with respect to crust (EF) = ,( /Ci CSi)Soil
( /Ci CSi)Crust
EF in soil with respect to background = ,( /Ci CSi)Soil
( /Ci CSi)BG
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Table 5
Enrichment factor (EF) of the trace elements in the top soils with respect to the crust
Elements
EF
1A 1B 4A 4B
Be 1.4 1.4 1.8 1.8
V 2.1 2.3 2.6 2.3
Cr 2.6 3.0 3.2 2.8
Mn 2.1 2.1 2.6 2.5
Ni 2.4 2.8 3.0 2.4
Co 1.8 1.9 2.8 2.1
Cu 2.5 3.0 3.5 2.5
Zn 1.8 2.4 2.5 1.7
As 1.9 2.2 3.8 2.3
Rb 1.5 1.5 1.8 1.7
Sr 0.4 0.4 0.4 0.4
Mo 3.8 5.7 5.8 4.7
Ba 1.2 1.2 1.2 1.2
Pb 1.1 1.2 1.8 1.3
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Table 6
Enrichment factor (EF) of the trace elements in the top soils with respect to the background
Elements
EF
1A 1B 4A 4B
Be 3.5 3.6 4.4 4.4
V 5.3 5.8 6.5 5.8
Cr 1.3 1.5 1.6 1.4
Mn 2.1 2.2 2.7 2.6
Ni 1.8 2.1 2.3 1.8
Co 0.9 1.0 1.5 1.1
Cu 4.1 4.8 5.6 4.1
Zn 3.7 4.9 5.2 3.4
As 2.7 3.1 5.4 3.4
Rb 1.1 1.1 1.3 1.3
Sr 1.1 1.1 1.3 1.1
Mo 0.9 1.3 1.3 1.1
Ba 4.5 4.8 4.9 4.7
Pb 1.5 1.5 2.4 1.7
From the above observations, it is inferred that Zn, Cu, Ni, Co, Mo, Mn, Cr, V,
and Ba are enriched in the topsoil around the ash pond to varying degrees
with respect to the crust as well as the background. Interestingly, all these
elements are enriched in concentration in the pond ash with respect to the
crust. Being fine grained (fine sand to silt sizes) the ash particles are easily
carried by the wind. These elements showed prominent enrichment in the topFirefox can't load web fonts from a remote host
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soils in the profiles within or close to the predominant wind direction, i.e. SW.
The ash ponds 1B, 4A and 4B are in the south westerly direction of the power
plant. Moreover the profiles from which soil samples were collected all lie to
the SW of the above mentioned ash ponds. Hence the soils from these profiles
show greater enrichment of trace elements due to input of ash blown by the
wind than those near ash pond 1A, which lies against the prevalent wind
direction. Since the profiles are in a south and south westerly direction of the
ash ponds, the top soils from these profiles show higher concentration of the
trace elements.
Log-normal distribution plots
Heavy metal distribution in sediments closely follow the log-normal law
(Sinclair 1981). The frequency distribution of pollutants in soils, sediments
could be examined using the log-normal distribution plots. Forstner (1983)
stated that background values, serving as thresholds between polluted and
unpolluted areas, can be derived from the log-normal distribution plots. For
metal distributions in which linearity is not observed, a break point
delineating inflection of the curve is arbitrarily fixed and the corresponding
concentration is used to represent an operational threshold between polluted
and non-polluted (or slightly polluted) areas. The theory of Sinclair have been
used in the present study to assess the extent of pollution of the soils of the
study area from the wastes of the power plants. Log-normal distribution plots
for element concentrations in surface soils of all the locations have been
delineated following Celo et al. (1998) and are shown in Fig. 5. From the plots
it is seen that the values of the square of the correlation coefficients (R 2)
range from 0.85 to 0.97.
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Fig. 5
Log-normal distribution plots of the trace elements in the top soils from the profiles near the ash ponds ofKolaghat thermal power plant
The distributions of Mn, As, Co, Cu, Pb, Ba, Ni shows poor linearity (R 2 are
0.85, 0.84, 0.90, 0.90, 0.90, 0.86, and 0.91, respectively), suggesting a
significant impact of anthropogenic activity in their distribution. The most
common source of anthropogenic activity in these areas is the disposal of ash
from the thermal power plant. The inflection point is well defined in the
distribution plots of the above mentioned trace elements. The other trace
elements Be, V, Cr, Rb, Sr Mo and Zn also show poor but slightly better
linearity (R 2=0.93, 0.94, 0.96, 0.97, 0.93, 0.93 and 0.95). Their distribution isFirefox can't load web fonts from a remote host
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23 of 29 Tuesday 17 February 2015 07:53 PM
also to a large extent affected by the polluting sources, but the contrast
between polluted and unpolluted sources with respect to the above mentioned
elements is not very well defined.
Conclusions
The present work thus show significant amount of contamination of the top
soil due to ash disposal. The contamination is more pronounced in the soils
within or close to the predominant wind direction. The concentrations of all
the trace elements in all the soil profiles around the ash pond are higher than
the background. The order of concentrations of Mn, Ba, V and Cr in profile
soils is similar to that found in pond ash. The physicochemical and
mineralogical properties of the profile soil in the predominant wind direction
are found to be modified compared to the background and other profile soils.
pH of the soil is lowered by the addition of ash from the power plant. A soil pH
below about 5.6 is considered low for most crops. At these low pH’s, the
solubility of aluminium, iron, and boron is high; Many heavy metals become
more water soluble under acid conditions and can move downward with water
through the soil, and in some cases move to aquifers, surface streams, or
lakes. Hence disposal of ash affects the agricultural quality of the soil.
Mullite, one of the major mineral phases in coal ash, has also been detected in
these soils. The anomalous presence of mullite in the profile soils has been
attributed to ash input through local anthropogenic activity, which was
observed in the field. Statistical treatment of the soil data further strengthens
the extent of contamination of the soils. This causes greater concern for
agricultural activities in the region which is located in a densely populated and
highly industrial zone Plants growing on these soils may incorporate theses
trace elements through uptake by the roots, and thus may enter into the food
chain of animals who consumes these plants. The metal input to the
surrounding topsoil is expected to continue unabated as the ash pond
continues to be filled more and more with the ash which ultimately forms the
topsoil. Praharaj et al. 2003 have also shown contamination of soil from ash of
a thermal power plant at Angul, Orissa. The soils near the ash ponds of Angul,
when analysed for trace elements showed that with respect to the crust, the
EF values of the trace elements were within the range of 0.2 to 31. The higher
values were for Mn (0.8–31.8) followed by Ba (1.4–8.1), Pb (1.5–6.3), V
(0.7–3.7), Cr (0.8–2.9), Cu (0.2–2.5), Zn (0.3–2.4), Co (0.4– 2.1) and NiFirefox can't load web fonts from a remote host
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(0.2–0.9). The enrichment of all the elements in the topsoil around the ash
pond is attributed to their input from ash from the disposal pond, almost
similar to the present work.
The present work thus helps to delineate the areas of contamination around
the ash ponds which will further help to develop remedial measures to combat
the problem.
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