Chapter Two Physical Characteristics of Soils
Chapter Two Physical Characteristics of Soils
Chapter Two Physical Characteristics of Soils
Chapter Two
2.1 Introduction
The purpose of this chapter is to introduce you to the physical prosperities soils.
You will learn some basic descriptions of soils and some fundamental physical soil
properties that you should retain for future use in this course and in geotechnical
engineering practice. Soils, derived from the weathering of rocks. One of the
primary tasks of a geotechnical engineer is to collect, classify and investigate the
physical properties of soils. In this chapter we will deal with descriptions of soils,
tests to determine the physical properties of soils, and soil classification systems.
When you complete this chapter you should be able to determine the following
terms in physical properties of soil:
Describe and classify soils.
Determine particle size distribution in a soil mass.
Determine the proportions of the main constituents in a soil.
Determine index properties of soil.
Determine colors, texture structure, specific gravity, relative density,
consistence limits etc…
'
Effective unit weight ( γ ) is the weight of soil solids in a submerged soil per unit
volume.
Relative density (Dr) is an index that quantifies the degree of packing between the
loosest and densest state of coarse-grained soils.
Effective particle size (D10) is the average particle diameter of the soil at 10
percentile; that is, 10% of the particles are smaller than this size (diameter).
Average particle diameter (D50) is the average particle diameter of the soil.
Liquid limit (wLL) is the water content at which a soil changes from a to plastic
state.
Plastic limit (wPL) is the water content at which a soil changes from a semisolid to
a plastic state.
Shrinkage limit (wSL) is the water content at which the soil changes from a solid to
a semisolid state without further change in volume.
We can idealize the three phases of soil as shown in Fig. 2.6b. The physical
properties of soils are affected by the relative proportions of each of these phases.
The total volume of the soil is the sum of the volume of solids (Vs.), volume of water
(Vw), and the volume of air (Va), that is:
V = Vs + V w + Va = V s + Vv (2.1)
Where Vv is the volume of voids. The weight of the soil is the sum of the weight of
solids (Ws), and weight of water (Ww). The weight of air is negligible. Thus,
W = Ws + W w (2.2)
The following definitions have been established to describe the proportion of each
constituent in soil. Each equation can be represented with different variables. The
most popular and convenient ones are given here. You should try to memorize
these definitions and equations.
1. Water content (w) is the ratio, often expressed by percentage, of the weight of
water to the weight of solids.
Ww
w = × 100 %
Ws (2.3)
The water content of a soil is found by weighing a sample of the soil and then
placing it in an oven at 110 ± 50C until the weight of the sample remains
constant; that is all the absorbed water is driven out. For most soils a constant
weight is achieved in about 24 hours. The soil is removed from the oven, cooled,
and then weighed to obtain the water content. You will later do an example on how
to measure and calculate the water content of a soil.
2. Void ratio (e) is the ratio of the volume of void space to the volume of solids.
Vv
e=
Vs (2.4)
3. Specific Volume (V’) is the volume of soil per unit volume of solids.
V
V' = =1+ e
Vs (2.5)
4. Porosity (n) is the ratio of the volume of voids to the total volume. Porosity is
usually expressed as a percentage.
Vv
n=
V (2.6)
Porosity and void ratio are related by the expression,
e
n=
1+e (2.7)
5. Specific gravity (Gs) is the ratio of the weight of the soil solids to the weight of
water of equal volume:
Ws
Gs =
V sγw (2.8)
Where
γ w = 9.81 kN/m3 is the unit weight of water. The specific gravity of soils
ranges from approximately 2.6 to 2.8. For most problems, Gs can be assumed, with
little error, to be equal to 2.7.
Two types of containers are used to determine the specific gravity. One is a
pycnometer, which is used for coarse-grained soils. The other is a 50 mL density
bottle, which is used for fine-grained soils. The container is weighed and a small
quantity of dry soil is placed in it. The mass of the container and the dry soil is
determined. De-aired water is added to the soil in the container. The container is
then agitated to remove air bubbles. When all air babbles has been removed the
container is filled with de-aired water. The mass of container, soil, and de-aired
water is determined. The contents of the container are discarded and the container
is thoroughly cleaned. De-aired water is added to fill the container and the mass of
the container and de-aired water is determined.
Let m1 be the mass of the container; m2 be the mass of the container and dry
soil; m3 be the mass of the container, soil, and water; and m4 be the mass of the
container and water. The mass of dry soil is ms = m2 – m1, the mass of water
displaced by the soil particles is m5 = m4 – m3 + ms and Gs = ms/m5.
Vw wG s
S= = or Se = wG s
Vv e (2.9)
7. Unit weight is the weight of a soil per unit volume. We will use the term bulk
unit weight, γ , to denote the unit weight of a soil:
W G + Se
γ=
V
= s (
1+ e w
γ ) (2.10)
Gs + e
γ sat = ( 1+e ) γw
(2.11)
Ws Gs γ
γd =
V
= ( )
1+e
γw =
1+w (2.12)
Gs − 1
γ ' = γ sat − γ w = ( 1+ e ) γw
(2.13)
Ge
' sat w w w
1 e
Ge G e 1 e
' 1 w w
1 e 1 e
G 1
' w
1 e
8. Relative Density (Dr) is an index that quantifies the degree of packing between
the loosest and densest possible state of coarse-grained soils as determined by
experiments:
e max − e
Dr =
e max − e min (2.14)
Where
e max is the maximum void ratio (loosest condition), e min is the
minimum void ratio (densest condition), and e is the current void ratio.
The maximum void ratio is found by dry sand, for example, into a mold of volume
(V) using a funnel. The sand that fills the mold is weighed. If the weight of the sand
is W, then by combining Eqs. (2.10) and (2.12) we get e max =G s γ w (V /W )−1 . The
minimum void ratio is determined by vibrating the sand with a weight imposing a
vertical stress of 13.8 kPa on top of the sand. Vibration occurs for 8 minutes at a
frequency of 3600 Hz and amplitude of 0.064 mm. From the weight of the sand
(W1) and the volume (V1) occupied by it after vibration, we can calculate the
Dr (%) Description
0 – 15 Very loose
15 – 35 Loose
35 – 65 Medium dense
65 – 85 Dense
85 – 100 Very dense
The relative density correlates very well with the strength of coarse-grained soils,
denser soils being stronger than looser soils. A description of sand based on
relative density is given in Table 2.2.
EXAMPLE 2.1
wG s γ
S= γd =
(a) e (b) 1+w
Gs + Se G s γ w (1 + w)
(c)
γ= ( 1+e ) γw =
1+e
EXAMPLE 2.2
A sample of saturated clay was placed in a container and weighed. The weight was
6 N. The clay in its container was placed for 24 hours at 105 0C. The weight reduced
to a constant value of 5 N. The weight of the container is 1 N. If G s = 2.7, determine
a) the water content, b) void ratio, c) bulk unit weight, d) dry density, and e)
effective unit weight.
EXAMPLE 2.3
An embankment for a highway is to be constructed from a soil compacted to a dry
unit weight of 18 KN/m3. The clay has to be trucked to the site from a borrow pit.
The bulk unit weight of the soil in the borrow pit is 17 KN/m 3 and its natural water
content is 5%. Calculate the volume of clay from the borrow pit required for 1 cubic
meter of embankment. Assume Gs = 2.7.
Strategy: This problem can be solved in many ways. We will here use two ways.
One way is direct; the other a bit longer. In the first way we are going to use the
ratio of the dry unit weights of the compacted soil and the borrow pit soil to
determine the volume. In the second way, we will use the specific volume. In this
case, we need to find the void ratio for the borrow pit clay and the desired void
ratio for the embankment. We can then relate the specific volumes of the
embankment and the borrow pit clay.
EXAMPLE 2.4
If the borrow soil in Example 2.3 were to be compacted to attain dry unit weight of
18 KN/m3 at a water content of 7%, determine the amount of water required per
cubic meter of embankment, assuming no loss of water during transportation.
Strategy: Since water content is related to the weight of solids and not the total
weight, we need to use the data given to find the weight of solids.
The main groups of crystalline minerals that make up clays are the minerals:
kaolinite, illite, and montmorillonite.
Kaolinite has a structure that consists of one silica sheet and one alumina sheet
bonded together into a layer about 0.72 nm thick stacked repeatedly (Fig. 2.3a).
The layers are held together by hydrogen bonds. Kaolinite is common in clays in
humid tropical regions.
Illite consists of repeated layers of one alumina sheet sandwiched by two silicate
sheets. The layers, each of thickness 0.96 nm, are held together by potassium ions.
Montmorillonite has similar structure to illite, but the layers are held together by
weak van der Waals forces and exchangeable ions. Water can easily enter the bond
and separate the layers resulting in swelling. Montmorillonite is often called
swelling or expansive clay.
Two common types of soil fabric, flocculated and dispersed, are formed during
soil deposition as schematically shown in Fig. 2.5. A flocculated structure,
Formed under a salt water environment, results when many particles are tend to
orient parallel to each other. A flocculated structure, formed under a freshwater
environment, results when many particles tend to orient perpendicular to each
other. A dispersed structure is the result when a majority of the particles orient
parallel to each other.
Any loading (tectonic or otherwise) during or after deposition permanently alters
the soil fabric or structural arrangement in a way that is unique to that particular
loading condition. Consequently, the history of loading and changes in the
environment is imprinted in the soil fabric. The soil fabric is the brain; it retains the
memory of the birth of the soil and subsequent changes that occur.
The spaces between the mineral particles are called voids, which may be filled with
liquids (essentially water) and gases (essentially air). Voids occupy a large
proportion of the soil volume. Interconnected voids form the passageway through
which water flows in and out of soils. If we change the volume of voids, we will
cause the soil to either compress (settle) or expand (dilate). Loads applied by a
building, for example, will cause the mineral particles to be forced closer together,
reducing the volume of voids and changing the orientation of the structural
framework. Consequently, the building settles. The amount of settlement depends
on how much we compress the volume of voids. The rate at which the settlement
occurs depends on the interconnectivity of the voids. Free water, not the adsorbed
water, and/or air trapped in the voids must be forced out for settlement to occur.
The decrease in volume, which results in settlement of buildings and other
structures, is usually very slow in fine-grained soils and almost ceaseless because
of their (fine-grained soils) large surface area compared with coarse-grained soils.
The large surface area in fine-grained soils compared to coarse-grained soils
provides greater resistance to the flow of water through the voids.
Fine-grained soils have poor load bearing capacities compared with coarse-grained
soils. Fine grained soils are practically impermeable, and change strength and
volume with variations in moisture conditions. The engineering properties of
coarse-grained soils are controlled mainly by the grain size of the particles and
their structural arrangement. The engineering properties of fine-grained soils are
controlled by mineralogical factors rather than grain size. Thin layers of fine-
grained soils, even within thick deposits of coarse-grained soils, have been
responsible for many geotechnical failures and therefore you need to pay special
attention to fine-grained soils.
A known weight of dry soil is placed on the largest sieve (the top sieve) and the
nest of sieves is then placed on a vibrator, called a sieve shaker, and shaken. The
nest of sieves is dismantled, one sieve at a time. The soil retained on each sieve is
weighed and the percentage of soil retained on each sieve is calculated. The results
are plotted on a graph of percent of particles finer than a given sieve (not the
percent retained) as the ordinate versus the logarithm of the particle sizes as
shown in Fig. 2.8. The resulting plot is called a particle size distribution curve (s)
or, simply, the gradation curve (s). Engineers have found it convenient to use a
logarithmic scale for particle size because the ratio of particle sizes from the
largest to the smallest in a soil can be greater than 104.
Let Wi be the weight of the soil retained on the ith sieve from the top of the nest of
sieves and W be the total soil weight. The percent weight retained is:
Wi
% Retained on i th seive = × 100
W (2.15)
The percent finer is:
i
% Finer than i th seive = 100 − ∑ (% Retained on i th seive)
i =1 (2.16)
You can use mass instead of weight. The unit of mass is in grams or kilograms.
The screening process cannot be used for fine-grained soils – silts and clays –
because of their extremely small size. The common laboratory method to
determine the size distribution of fine-grained soils is the hydrometer test (Fig.
2.9). The hydrometer test involves mixing a small amount of soil into suspension
and observing how the suspension settles in time. Larger particles will settle
quickly followed by smaller particles. When the hydrometer is lowered into the
suspension, it will sink into the suspension until the buoyant force is sufficient to
balance the weight of the hydrometer. The calibration of hydrometer is affected by
temperature and specific gravity of the suspended solids. You must then apply a
correlation factor to your hydrometer reading based on the test temperatures.
18μz
D=
√ (G s − 1)γ w t D (2.17)
Where μ is the viscosity of water (10.09 mill poises at 20 0C), z is the depth,
γ w is the unit weight of water, and G is the specific gravity. The dashed line in
s
Fig. 2.8 shows a typical particle size distribution for fine-grained soils.
The grading curve is used for textural classification of soils. Various classification
systems have evolved over the years to describe soils based on their particle size.
The Unified Soil Classification System (USCS) – which we will discuss in detail in
section 2.7 – is one of most common methods. The USCS separates soils into two
categories. One category is coarse-grained soils that are delineated if more than
50% of the soil is greater than 0.075 mm (No. 200 sieve). The other category is
fine-grained soils that are delineated if more than 50% of the soil is finer than
0.075 mm. Coarse-grained soils are subdivided into gravels and sands while fine-
grained soils are divided into silts and clays. Each soil type – gravel, sand, silt, and
clay – is identified by grain size as shown in table 2.3. The USCS does not
differentiate silts from clays. Clays have particle sizes less than 0.002 mm
Real soils consist of a mixture of particle sizes. The selection of a soil for a
particular use may depend on the assortment of particles it contains. Two
coefficients have been defined to provide guidance on distinguishing soils based on
the distribution of the particles. One of these is a numerical measure of uniformity,
called the uniformity coefficient, UC, defined as:
D60
UC =
D10 (2.18)
Where D60 is the diameter of the soil particles for which 60% of the particles are
finer, and D10 is the diameter of the soil particles for which 10% of the particles are
finer. Both of these diameters are obtained from the grading curve.
The other coefficient is the coefficient of curvature, CC (other terms used are the
coefficient of gradation and the coefficient of concavity), defined as:
2
( D30 )
CC =
D10 D60 (2.19)
Where D30 is the diameter of the soil particles for which 30% of the particles are
finer. A soil that has a UC < 4 contains particles of uniform sizes (approximately one
size). The minimum value of UC is 1 and corresponds to an assemblage of particles
of the same size. The gradation curve for a uniform soil is almost vertical (Fig. 2.8).
Higher values of UC (> 4) indicate a wider assortment of particle sizes. A soil that
has a UC > 4 is described as a well-graded soil and has a flat curve (Fig. 2.8). The CC
is between 1 and 3 for well-graded soils. The absence of certain grain sizes, termed
gap-graded, is diagnosed by a CC outside of the range 1 to 3 and a sudden change of
slope in the particle size distribution cure as shown in Fig. 2.8.
Table 2.3: Soil types, descriptions, and average grain sizes according to USCS
The diameter D10 is called the effective size of the soil and was established by
Allen Hazen (1893) in connection with his work on soil filters. The effective size is
particularly important in regulating the flow of water through soils. The higher the
D10 value are the coarser the soil and the better the drainage characteristics. The
diameter of the finer particle sizes, in particular D15, has been used to develop
criteria for soil filters. Terzaghi and Peck (1948), for example, proposed the
following set of criteria for an effective soil filter:
D15( F )
< 4 (to prevent filter soil from being washed away )
D 85( BS )
And
D15( F )
> 4 ( to ensure a higher rate of flow water )
D15 ( BS )
Where F denotes filter and BS is the base soil. The average diameter of a soil is
given as D50. Particle size analysis has many uses in engineering. They are used to
select aggregates for concrete, soils for the construction of dams and highways,
soils as filters, and material for grouting and chemical injection.
EXAMPLE 2.5
A sample of dry coarse-grained material of mass 500 grams was shaken through a
nest of sieves and the following results were obtained:
4 4.75 0
10 2.00 14.8
20 0.85 98
40 0.425 90.1
100 0.15 181.9
200 0.075 108.8
Pan 6.1
(b)Determine (1) the effective size, (2) the average particle size, (3) the uniformity
coefficient, and (4) the coefficient of curvature.
(c) Determine the textural composition of the soil (i.e. the amount of gravel, sand,
etc.).
Strategy: the best way to solve this type of problem is to make a table to carry out
the calculation and then plot a gradation curve. Total mass of dry sample (M) used
is 500 grams but on summing the masses of the retained soil in column 2 we obtain
499.7 grams. The reduction in mass is due to losses mainly from a small quantity of
soil that gets stuck in the meshes of the sieves. You should use the “after sieving”
total mass of 499.7 grams in the calculations.
The physical and mechanical behavior of fine-grained soils is linked to four distinct
states – solid, semisolid, plastic, and liquid – in order of increasing water content.
Let us consider a soil in a liquid state that is allowed to dry uniformly. If we plot a
diagram of volume versus water content as shown in Fig. 2.10, we can locate the
original liquid state as point A. as the solid dries its water content reduces and
consequently its volume.
Figure 2.10: Change in soil states as a function of soil volume and water content.
At point B, the soil becomes so stiff that it can no longer flow as a liquid. The
boundary water at point B is called the liquid limit; it is denoted by wLL. As the soil
continues to dry, there is a range of water content at which the soil can be molded
into any desired shape without rapture. The soil at this state is said to exhibit
plastic behavior – the ability to deform continuously without rapture. But if drying
is continued beyond the range of water content for plastic behavior, the soil
becomes a semisolid. The soil can not be molded now without visible cracks
appearing. The water content at which the soil changes from a plastic to a
semisolid state is known as the plastic limit, denoted by wPL. The range of the
water contents over which the soil deforms plastically is known as the plasticity
index, IP:
I P = w LL − w PL (2.20)
As the soil continues to dry, it comes to a final state called the solid state. At this
state, no further volume change occurs since nearly all the water in the soil has
been removed. The water content at which the soil changes from the semisolid to a
solid is called the shrinkage limit, denoted by wSL. The shrinkage limit is useful for
the determination of the swelling and shrinkage capacity of soils. The liquid and
plastic limits are called Atterberg limits (also known as consistency limits). The
Atterberg limits were originated by a Swedish soil scientist, A. Atterberg (1911).
w − w PL
IL =
IP (2.21)
The liquidity index is the ratio of the difference in water content between the
natural (or in situ) water content of a soil and its plastic limit to its plasticity index.
Table 2.4 shows a description of soil strength based on values of IL.
Typical values for the Atterberg limits for soils are shown in Table 2.5. The
Atterberg limits depend on the type of predominant mineral in the soil. If
montmorillonite is the predominant material, the liquid limit can exceed 100%.
Why? Recall that the bond between the layers in montmorillonite is weak and large
amounts of water can easily infiltrate the spaces between the layers. In the case of
kaolinite, the layers are held relatively tightly and water cannot easily infiltrate
between the layers in comparison with montmorillonite. Therefore, you can expect
the Atterberg limits for kaolinite to be, in general, much lower than either
montmorillonite or illite.
Skempton (1953) showed that for soils with a particular mineralogy, the plasticity
index is linearly related to the amount of the clay fraction. He coined a term called
activity (A) to describe the importance of the clay fractions on the plasticity index.
The equation for A is:
IP
A=
Clay fraction (%)
You should recall that the clay fraction is the amount of particles less than 2μm.
Skempton classified clays according to Table 2.6
A Description
The apparatus was discovered by A. Casagrande (1932) and the procedure for the
test is called the Casagrande cup method.
A dry powder of the soil is mixed with distilled water into a paste and
placed in the cup to a thickness of about 12.5 mm. The soil surface is smoothed and
a groove is cut into the soil using a standard grooving tool. The crank operating the
cam is turned at a rate of 2 revolutions per second and the number of blows
required to close the groove over a length of 12.5 mm is counted and recorded. A
specimen of soil within the closed portion is extracted for determination of the
water content. The liquid limit is defined as the water content at which the groove
cut into the soil will close over a distance of 12.5 mm following 25 blows. This is
difficult to achieve in a single test. Four or more tests at different water contents
are usually required for terminal (number of blows to close the groove over a
distance of 12.5 mm) ranging from 10 to 40. The results are presented in a plot of
water content (ordinate, arithmetic scale) versus terminal blows (abscissa,
logarithmic scale) as shown in Fig. 2.12.
Figure 2.12: Typical liquid limit results from the Casagrande cup method.
The best-fit straight line to the data points, usually called the flow line, is
drawn. We will call this line the liquid state line to distinguish it from flow lines
used in describing flow of water through soils. The liquid limit is read from the
graph as the water content on the liquid state line corresponding to 25 blows. The
cup method of determining the liquid limit has many shortcomings. Two of these
are:
1. The tendency of soils of low plasticity to slide and to liquefy with shock in the
cup rather than to flow plastically.
The plastic limit is determined by rolling a small clay sample into threads
and finding the water content at which threads approximately 3 mm in diameter
will just start to crumble. Two or more determinations are made and the average
water content is reported as the plastic limit.
Larger than the smaller cone mass of 80 grams. Thus the liquid state line for the
240 gram cone will be below the liquid state line for the 80 gram cone and parallel
to it. The plastic limit is given as:
2 Δw
w PL = w LL − = w LL − 4 .2 Δw
log 10 ( M 2 / M 1 ) (2.22)
Where Δw is the separation in terms of water content between the liquid state
lines (Fig. 2.14) of the two cones, M1 is the mass of 80 grams cone, and M2 is the
mass of the 240 gram cone.
80 gram cone
wLL=44%
D. Shrinkage Limit
The shrinkage limit is determined as follows. A mass of wet soil, m1, is placed
in a porcelain dish 44.5 mm in diameter and 12.5 mm high and then oven-dried.
The volume of oven-dried soil is determined by using mercury to occupy the
vacant spaces caused by shrinkage. The mass of the mercury is determined and
the volume decrease caused by shrinkage can be calculated from the density of
mercury. The shrinkage limit is calculated from:
m1 − m2 V 1 − V 2 γ w
w SL =
( m2
−
m2 g )
× 100
(2.23)
Where m1 is the mass of the wet soil, m2 is the mass of the oven-dried soil, V1 is the
volume of the wet soil, V2 is the volume of the oven-dried soil, and g is the
acceleration due to gravity (9.8 m/s2).
EXAMPLE 2.6
A liquid limit test conducted on a soil sample in the cup device gave the following
results.
Number of blows 10 19 23 27 40
Water content 60.0 45.2 39.8 36.5 25.2
(%)
Two determinations for the plastic limit gave water contents of 20.3% and 20.8%.
Determine (a) the liquid limit and plastic limit, (b) the plasticity index, (c) the
liquidity index if the natural water content is 27.4 %, and (d) void ratio at the
liquid limit, if Gs = 2.7. If the soil were to be loaded to failure, would you expect a
brittle failure?
Strategy: To get the liquid limit, you must make a semi-logarithm plot of water
content versus number of blows. Use the data to make your plot, then extract the
liquid limit (water content on the liquid state line corresponding to 25 blows).
Two determinations of the plastic limit were made and the differences in the
results are small. So, use the average value of water content as a plastic limit.
EXAMPLE 2.7
The results of a fall cone test are shown in the table below.
Determine (a) the liquid limit, (b) the plastic limit, (c) the plasticity index, and (d)
the liquidity index if the natural water content is 36%.
Strategy: Adopt the same strategy as in Example 2.6. Make a semi-logarithm plot
of water content versus penetration. Use the data to make your plot, then extract
the liquid limit (water content on the liquid state line corresponding to 20 mm).
Find the water content difference between the two liquid state lines at any fixed
penetration. Use this value to determine the plastic limit.
was found that clays, silts, and organic soils lie in distinct regions of the graph. A
line defined by the equation,
called the “A-line,” delineates the boundaries between clays (above the line) and
silts and organic soils (below the line) as shown in Fig. 2.16. A second line, the U-
line expressed as IP = 0.9(wLL – 8), defines the upper limit of the correlation
between plasticity index and liquid limit. If the results of you soil tests fall above
the U-line, you should be suspicious of your results and repeat your tests.
60
Comparing soils at equal liquid limit
50 Toughness and dry strength increase
with increasing plasticity index
40
Plasticity index
CH
30
20 OH
CL or
10 CL OL
or MH
ML
0 ML
0 10 20 30 40 50 60 70 80 90 100
Liquid limit
Plasticity chart
for laboratory classification of fine grained soils
Figure 2.16: Plasticity chart.
laboratory tests namely, sieve analysis liquid limit and plastic limit.
Soils are divided into seven groups A-1 to A-7. A-1, A-2, and A-3 soils are granular
soils, percentage fines passing 0.074mm sieve being less than 35. A-4, A-5, A-6, and
A-7, soils are fine grained or silt-clay soils, passing 0.074 mm sieve being greater
than 35 percent.
A-1 soils are well graded mixture of stone fragments, gravel coarse sand, fine sand
and non-plastic or slightly plastic soil binder. The soils of this group are subdivided
into two sub-groups, A-1-a consisting predominantly of stone fragments or gravel
and A-1-b consisting predominantly of coarse sand.
A-2 group of soils include a wide range of granular soils ranging from A-1 to A-3
groups, consisting of granular soils and up to 35% fines of A-4, A-5, A-6 or A-7
groups. Based on the fines content, the soils of A-2 groups are subdivided into
subgroups A-2-4, A-2-5, A-2-6 and A-2-7.
A-3 soils consist mainly, uniformly graded medium or fine sand similar to beach
sand or desert blown sand. Stream deposited mixtures of poorly graded fine sand
with some coarse sand and gravel are also included in this group.
A-4 soils are generally silty soils, non-plastic or moderately plastic in nature with
liquid limit and plasticity index values less than 40 and 10 respectively.
A-5 soils are also silty soils with plasticity index less than 10%, but with liquid limit
values exceeding 40%. These include: highly elastic or compressible soils.
A-6 group of soils are plastic clays, having high values of plasticity index exceeding
10% and low values of liquid limit below 40%; they have high volume change
properties with variation in moisture content.
A-7 soils are also clayey soils as A-6 soils, but with high values of both liquid limit
and plasticity index, (LL greater than 40% and PI greater than 10%). These soils
have low permeability and high volume change properties with changes in
moisture content.
Fine grained soils of each classification group exhibit a wide range of properties as
sub-grade material.
In order to classify the fine grained soils within one group and for judging their
suitability as sub-grade material, an indexing system has been introduced in HBR
classification which is termed as Group Index. Soils are thus assigned arbitrary
numerical values known as group index (GI).
Group Index is function of percentage material passing 200 mesh sieve (0.074mm),
liquid limit and plasticity index of soil and is given by the equation:
GI=0.2a+0.005ac+0.01bd
Where
a=the portion of material passing 0.074mm sieve, greater than 35 and not
exceeding 75% (expressed as a whole number from 0 to 40).
b=that portion of material passing 0.074mm sieve greater than 15 and not
exceeding 35% (expressed as a whole number from 0 to 40).
c=that value of liquid limit in excess of 40 and less than 60(expressed as a
whole number from 0 to 20)
d=that value of plasticity index exceeding 10 and not more than 30
(expressed as a whole number from 0 to 20)
According to this formula, the minimum possible value of group index is zero and
the maximum possible value is 20, when the values of soil fraction passing
0.074mm sieve, liquid limit and plasticity index are respectively higher than 75, 60
and 30 %. Higher the value of group index, poorer is the soil sub-grade material.
The sub-groups A-2-6 and A-2-7 soils of A-2 group have GI values 0 to 4, A-4 group
of soil have GI values up to 8; A-5 soil up to 12, A-6 soil up to 16 and A-7 soil up to
20. The group index value is indicated as suffix to the soil group within brackets,
such as A-6(4) or A-6(16).
You may ask “How do I use a soil classification to select a soil for a particular type
of construction, for example, a dam?” Geotechnical engineers have prepared charts
based on experience to assist you in selecting a soil for a particular construction
purpose. One that chart is shown in Table 2.7. The numerical values 1 to 9 are
ratings with No. 1 the best. The chart should only be used to provide guidance and
to a preliminary assessment of the suitability of a soil for a particular use. You
should not rely on such descriptions as “excellent” shear strength or “negligible”
compressibility to make the final design and construction decisions. You will learn
later more reliable method to determine strength and compressibility properties.
Important property
no fines.
EXAMPLE 2.8
Particle size analyses were carried out on two soils – Soil A and Soil B – and the
particle size distribution curves are shown in Fig. E2.8 below. The Atterberg limits
Figure E2.8: Particle size distribution curves for soil A and soil B.
(a) Classify these soils according to the Unified Soil Classification System.
(b) Is either of the soils organic?
(c) In a preliminary assessment, which of the two soils is a better material for the
core of a rolled earth dam?
Strategy: If you examine the flowcharts of Figs. 2.15 a and b, you will notice that
you need to identify the various soil types based on texture: for example, the
percentage of gravel or sand. Use the particle size distribution curves to extract
the different percentages of each soil type and then follow the flowchart. To
determine whether your soil is organic or inorganic, plot your Atterberg limits on
the plasticity chart and check whether the limits fall within an inorganic or
organic soil region.