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INTRODUCTION:
Soil is among our most significant natural resources because of its position in the
landscape and its dynamic, physical, chemical and biological functions. When the soil
accumulates heavy metals beyond a level, it becomes contaminated. The term ‘heavy
metal’states to any metallic chemical component that has a relatively high density and is toxic
or poisonous at low concentrations. Heavy metals are generally defined as those having a
specific density of more than 5 g/cm3. Heavy metals show metallic properties such as
malleability, ductility, cation stability, conductivity, and ligand specificity. They are also
considered by relatively high atomic weight with an atomic number greater than 20.
Soils accumulate heavy metals in two ways: One is natural and the other
anthropogenic. Examples of natural sources of contamination include: seepage from rocks
into water, volcanic activity, and forest fires. However, heavy metals from these natural
sources rarely reach toxic levels. The primary source of heavy metal contamination is
anthropogenic that include consumerist lifestyle, emissions from the rapidly expanding
industrial activities, mine tailings, disposal of high metal wastes, leaded gasoline, paints, land
application of fertilizers, animal manures, sewage sludge, pesticides, wastewater irrigation,
coal combustion residues, spillage of petrochemicals, and so on. Thus, contamination
happens throughout economic activities and life cycles of products - from production, usage,
and disposal.
Soil contamination is not only harmful for the subsurface water aquifers but also for
structures existing on it. Any changes in the engineering properties and behaviour of soil
strata may lead to a loss of bearing capacity, an increase in total or differential settlement of
foundation system of structures, leading ultimately to failure of structures. In India, the
prominent heavy metal contaminants are lead, mercury, chromium, cadmium, copper and
aluminium. Many urban and dense Indian cities with significant industrial waste generation
have been found to have contaminated soil. (CPCB, 2009).
Heavy metals are found to exist in soil either as separate entities or as combined soil
components - that is, heavy metals can combine with various soil components such as
exchangeable ions that are sorbed on the surfaces of inorganic solids, non-exchangeable ions,
insoluble inorganic metal compounds (examples: carbonates and phosphates), soluble metal
compounds, free metal ions, and metals of organic matter and silicate materials. The
presence of heavy metals varies from soil to soil, depending on factors such as soil pH, the
density of soil, type of charge in soil colloids, degree of complexation with ligands, and
relative surface area. The concentrations of the heavy metals depend on the soil’s adsorption
property, which comes from the organic matter present in the soil. The functional groups of
the organic matter like phenolic group are capable of complexing with heavy metals.
Environmental factors like land use, temperature, and rainfall can change the content of the
organic matter and concentration of heavy metals.
The adverse impacts of heavy metal contaminants on the index and engineering
properties of the soil is not widely studied when compared to the environmental degradation
or the agricultural or human health issues that arise out of heavy metal contamination of soil.
This comprehensive study is undertaken to find the impact of three different types of heavy
metal contaminants - namely, lead, copper, and chromium, - on the engineering properties of
black cotton soil, under lab environments. The study documents the variations in the
geotechnical properties - including shear strength, compressibility, permeability and
compaction capacity - of the contaminated soil against that of the virgin soil.
The study is based on the exposure of virgin soil to the 500 ppm, 1000 ppm, and 2000
ppm concentrations of the three aforementioned heavy metals separately for the duration of 7,
14, and 28 days. In addition, Atomic Absorption Spectrophotometer tests were done on the
contaminated black cotton soil to find the residual concentration of lead, copper, and
chromium in 500 ppm, 1000 ppm, and 2000 ppm concentrations involving a curing period of
30 days. The study finds that the level of contamination is closely associated with the
chemical composition of the contaminants and the physical properties of the soil. The
findings can help engineers to evaluate the characteristics and behaviour of contaminated soil
predictively, and optimize the safety and stability of the structures they design on or below
the contaminated soil.
In the context of increasing scarcity of land, there is a need to make use of even
contaminated soil for construction if safety of the structures can be ensured. The objective of
the study is to understand the changes in the index and geotechnical / engineering properties
of soil - under lab environment, using scientific methods, after artificially contaminating the
soil with heavy metal contaminants at various concentrations and curing periods. The study
also aims to find the residual concentration of lead, copper, and chromium with varying
concentrations. The findings of the study should help engineers predict the possible
behavioural changes of heavy metal contaminated soil and incorporate safety measures to the
structures they build on or under contaminated soil.
MATERIALS & METHODS:
The study is based on black cotton soil and three heavy metal contaminants lead,
copper, and chromium. The representative disturbed black cotton soil samples for the purpose
of the study were acquired from Thirumangalam, Madurai. The soil samples were tested for
basic index properties as per IS 2720: 1991. The property of uncontaminated soil is tabulated
in table 1. The analytical reagent grade salts of lead nitrate, copper sulphate, and chromium
nitrate were procured to make the solutions of lead, copper, and chromium respectively, and
in the required concentrations. The black cotton soils were taken in different polyethylene
bags, and were in turn kept in separate containers - one each for a heavy metal of a particular
concentration. The levels of concentrations of heavy metals taken for the study were 500
ppm, 1000 ppm, and 2000 ppm. These artificially contaminated soils were subjected to the
curing periods of 7, 14, and 28 days. Comparable tests were done also for uncontaminated
soils. After the curing periods, the index and geotechnical / engineering properties of the
contaminated soils were analysed. The analyses were done for consistency limits, free swell
index, compressibility characters, and permeability, among others, as per IS 2770:1991 -
Parts 5, 6, 10. 15 & 40.
Table 1 Properties of uncontaminated soil
Property Value
Specific gravity 2.64
Particle size analysis
Sand % 19
Silt % 28
Clay % 53
Atterberg’s Limits
Liquid Limit % 82
Plastic Limit % 39
Plasticity Index % 43
Shrinkage Limit % 15
IS Classification CH
Differential free swell index
F.S.I % 63.15
Chemical Properties
pH 8.14
Organic matter % 2.25
Cation exchange capacity mq/100 g 17.38
Compaction test results
Optimum moisture content % 19
Maximum Dry Density g/cc 1.661
Other Properties
Electrical Conductivity (ms/cm) 0.721
Table 1 summarizes various index properties of uncontaminated soil. The specific
gravity of uncontaminated soil is 2.64. The uncontaminated soil is composed of 19% of sand
and 81% of fines. The clay content is found to be 53%. As per IS classification the soil is
classified as clay of high plasticity (CH). The maximum dry density at standard Proctor
energy is 1.67 g/cc and the optimum moisture content of the uncontaminated soil is found to
be 19%.
In addition, Atomic Absorption Spectrophotometer tests were also done on the contaminated
black cotton soil. For this purpose, the soils were soaked in the solutions of each heavy metal
contaminant separately. The concentrations for all three contaminants were 500 ppm, 1000
ppm and 2000 ppm. The soaked soils were left undisturbed for adsorption - barring
occasional stirring, for 30 days. After the curing period, the contaminated soils were taken
out of the solution. They were then dried, and powdered to pass through 4.25 micron IS sieve.
The soils thus collected were analysed for residual concentration of lead (Pb), cobber (Cu)
and chromium (Cr) using Atomic Absorption Spectrophotometer (Perkin Elmer, Model
2380). The results obtained are presented in the following section.
It was also observed that the values of consistency limits were not appreciably affected at low
concentrations of heavy metals. Results obtained indicate that when the soil was
contaminated with high concentrations of heavy metals, the diffuse double layer thickness
decreases. This in turn results in the reduction in liquid limit, plastic limit and shrinkage limit.
Free Swell Index of contaminated soil:
The free swell index of uncontaminated and contaminated soil specimens was
determined as per Indian Standards (IS 2720 Part 40-1977) and the results are presented in
Table 3. Results obtained indicate that due to contamination, the free swell index of clayey
soils decreases. This also may be attributed to the reduction in the diffused double layer
thickness and is in line with the observed behaviour of the Atterberg Limits.
80 40
Liquid Limit (%)
60 30
40 20
20 10
0 0
500 1000 2000 500 1000 2000
Concentrations (ppm) Concentrations (ppm)
20 50
Shrinkage Limit (%)
15 40
30
10
20
5 10
0 0
500 1000 2000 500 1000 2000
Concentrations (ppm) Concentrations (ppm)
Fig 1. The results of various tests on consistency limit of soil for 7, 14 and 28 days of
contamination. (Method of Saturation)
Lead Nitrate – 7 Days Copper Sulphate – 7 Days Chromium Nitrate – 7 Days
Lead Nitrate – 14 Days Copper Sulphate – 14 Days Chromium Nitrate – 14 Days
Lead Nitrate – 28 Days Copper Sulphate – 28 Days Chromium Nitrate – 28 Days
2.5 3
2
Stress kg/sq.cm
Stress kg/sq.cm
Stress kg/sq.cm
2.5
2
1.5 0 ppm 0 ppm 2 0 ppm
1.5
1 500 ppm 500 ppm 1.5 500 ppm
1
1000 ppm 1000 ppm 1 1000 ppm
0.5 0.5
2000 ppm 2000 ppm 0.5 2000 ppm
0 0 0
0.00 20.00 40.00 60.00 0.00 20.00 40.00 60.00 0.00 20.00 40.00 60.00
Strain (%) Strain (%) Strain (%)
Lead Nitrate- Contamination Periods - 7 Days Lead Nitrate- Contamination Periods - 14 Days Lead Nitrate- Contamination Periods - 28 Days
3 3 3.5
2.5 2.5 3
Stress kg/sq.cm
Stress kg/sq.cm
Stress kg/sq.cm
2.5
2 2
0 ppm 0 ppm 2 0 ppm
1.5 1.5
500 ppm 500 ppm 1.5 500 ppm
1 1
1000 ppm 1000 ppm 1 1000 ppm
0.5 0.5 2000 ppm 0.5 2000 ppm
2000 ppm
0 0 0
0.00 20.00 40.00 60.00 0.00 20.00 40.00 60.00 0.00 20.00 40.00 60.00
Strain (%) Strain (%) Strain (%)
Copper Sulphate- Contamination Periods - 7 Days Copper Sulphate - Contamination Periods - 14 Days Copper Sulphate- Contamination Periods - 28 Days
2 2.5 3.00
2 2.50
Stress kg/sq.cm
Stress kg/sq.cm
Stress kg/sq.cm
1.5
2.00
0 ppm 1.5 0 ppm 0 ppm
1 1.50
500 ppm 1 500 ppm 500 ppm
1.00
0.5 1000 ppm 1000 ppm 1000 ppm
0.5 0.50
2000 ppm 2000 ppm 2000 ppm
0 0 0.00
0.00 20.00 40.00 60.00 0.00 20.00 40.00 60.00 0.00 20.00 40.00 60.00
Strain (%) Strain (%) Strain (%)
Chromium Nitrate- Contamination Periods - 7 Days Chromium Nitrate- Contamination Periods - 14 Days Chromium Nitrate- Contamination Periods - 28 Days
qu= Unconfined compression Test of Soil (Kpa), Cv= Coefficient of Consolidation (cm2/sec x
104), k = Coefficient of permeability(cm/secx108), c = Cohesiveness (kPa), Ф = Angle of
Internal friction (degrees)
Direct Shear Test of contaminated soil:
Direct Shear tests were carried out using uncontaminated and contaminated soil
specimens. The water content was maintained at 26% and the re-moulding density at
15kN/m3. The maximum shear stress and corresponding longitudinal displacement readings
were obtained. It can be seen that the angle of internal friction and cohesiveness decreased
with increase in the level of contamination of these soils. The variation of cohesions and
angle of internal frictions on lead, copper and chromium with different contamination periods
are summarized in Table 4.
DOMINATING MECHANISMS:
Lead, Copper and Chromium are strongly adsorbed to soil particles and therefore have very
little mobility relative to other trace metals. As a result of this limited mobility, applied
metals tend to accumulate in soil. Soil types have finite holding capacities for lead, copper
and chromium ions, factors that influence the availability of lead, copper and chromium in
soils are pH, cation exchange capacity (CEC), organic matter content, presence of oxides of
iron, manganese, and aluminium, the capacity of soil to adsorb these metals increased with
increasing pH, with a maximum holding capacity at neutral to slightly alkaline conditions
(pH 6.7–7.8). Furthermore, soils with alkaline conditions tend to favour precipitation of lead,
copper and chromium; thus, these metals are more mobile under acidic than alkaline
conditions.In general, the higher the CEC, the greater the amount of metal it can adsorb. The
CEC is influenced by the type and amount of clay present, the amount of organic matter
present, and the pH of the soil. Lead, Copper and Chromium have a very high affinity for
organic matter and are more strongly bound than other trace elements.
CONCLUSIONS:
A series of laboratory tests were conducted in order to find out the effect of index,
engineering and chemical properties on lead, copper and chromium contaminated soils. Tests
were conducted in such a way that considering different concentrations of contaminants as
well as different curing periods. It was found that various index, engineering and chemical
properties were affected due to the adsorption of heavy metals into soil. As the concentration
of the metal solution increases, the amount of adsorbed also increases to certain extent. Since
adsorption of heavy metal in clayey soils causes flocculation and an increase in the strength
characteristics of the soil. Distinct changes in soil properties were noticed for clayey soils
contaminated with higher concentrations of lead, copper and chromium contaminated soil.
The conclusions drawn from the current study are summarized below. Contamination of
clayey soils with lead, copper and chromium causes
Contamination of clayey soils with heavy metals cause reduction in liquid limit,
plastic limit and Shrinkage limit was also getting decreased, but there is no
appreciable reduction.
By comparing the free swell index values of uncontaminated and contaminated soil
samples, it was found that contamination of clayey soil with heavy metals reduce the
swelling properties.
It is essential to note that the strength of the lead, copper and chromium
contaminated soils increases till 1000ppm and beyond that, the strength of soil
decreased for 2000ppm.This phenomenon is due to the Adsorption capacity of
soil is higher at lower concentration, resulting more metals adsorption. This
also indicates that the sites for adsorption on this soil are still available at lower
concentration. This also indicates that the sites for adsorption on this soil are
still available at lower concentration. When the Adsorption sites become
saturated with metal solutions, the adsorption decreases with further increasing
of lead, copper and chromium in the solutions and thus the strength starts
decreasing.
So finally the conclusion arrives from this study is that the effect of heavy metal
contamination on geotechnical properties of black cotton soil is negligible for lower
concentrations. Hence, if heavy metal is within the levels of Environmental Protection
Agency (EPA), the heavy metals contaminated soils can be used as a good bearing material
itself, but in case of higher concentrations of heavy metals in soils, further remedial measures
shall be done to improve the engineering characteristics of soil.
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