Professional Documents
Culture Documents
Session 2012/2013
January 2013
G1
Index Properties, Soil Classification and
Consolidation
[CE 2112: Engineering Geology and Soil Mechanics]
1. Principles of Soil Classification
Rocks in the crust are subject to weathering and erosion (denudation) with time. Soils, the product of
denudation, form from transported material or in-situ decomposed rocks on the surface of the earth.
Because soil is a natural product (as opposed to concrete and steel, which were man-made), the
range of soil types and variety is enormous. Much of geotechnical engineering is founded on the basis
that, notwithstanding the wide variety of soils and properties that exists, their engineering behaviour is
generally governed by a few important parameters which are the object of geotechnical testing.
One of the basic sub-division of soils is that which classifies soil into sand and gravel (i.e. coarse
grained material), silt (i.e. intermediate-sized grain) and clay (fine-grained material). The system
which is used to classify sand and gravel into various sub-types is very different from that used to
classify silt and clay. This difference stems from the different factors affecting the behaviour of the
different soil types. Sand and gravel generally do not possess any chemical on their particle surfaces,
and the major factor affecting their behaviour is the particle size distribution. For this reason, sand
and gravel are often sub-classify on the basis of their particle size distribution. On the other hand, the
behaviour of finer-grained soils such as silt and clay is more significantly affected by surface activity
such as cation exchange and diffuse double layer, owing to the much larger surface area:volume ratio.
This fact was recognized and used by Atterberg (an agricultural scientist) to develop simple
classification tests which can define the activity of fine-grained soil. In this experiment, we will learn
about some simple tests which can be used to evaluate the Atterberg limits.
2. Atterberg Limits
2.1
Principles
Atterberg found that the activity of a soil can be succinctly defined by measuring three limiting water
contents [Water content = mass of water/mass of soil solids]. Starting with a fine-grained soil which
is almost fluid (which we generally call a slurry), as the water content is reduced, a point will be
reached at which the soil ceases to flow like a liquid and starts to take on characteristics of a solid
e.g. having a measurable strength. The water content at this point is known as the liquid limit (LL).
Further loss of water beyond this point enhances the solid characteristics further, with the shear
strength of the soil increasing and its volume decreasing as water content reduces. Throughout this
regime, the soil behaves as a pliable and ductile solid mass, similar in consistency to plasticine.
However, if loss of water is continued, another point will be reached at which the soil changes from a
pliable, ductile solid to a brittle solid, which tends to crack and break up when remoulded. The water
content at this point is known as the plastic limit (PL). Further drying reduces the volume even
5
further until the shrinkage limit (SL) is reached. Beyond this limiting water content, the soil is so
hard that further drying effectively produces no further volume change. Beyond this point, any loss of
water results in the voids being replaced by air. The range of water content between the liquid and
plastic limits is known as the plasticity index (PI), that is
PI = LL PL
(1)
While the shrinkage limit is lesser used, the liquid and plastic limits are two of the most commonly
measured soil classification parameters for fine-grained soils. Certain basic trends can be easily
discerned in the way the liquid and plastic limits changes with soil types and activity. These include
the following:
1. Liquid limit increases with activity of soil. A soil which is highly active (or highly plastic) can
adsorb a lot of water onto its surface before there is enough free water to cause it to flow like a
liquid.
2. For the same liquid limit, a soil that has larger particles tends to crumble or break up in a brittle
fashion more easily as water content reduces, and therefore generally has a higher plastic limit. In
other words, given the same liquid limit, a soil with larger particles will also tend to have a smaller
plasticity index.
2.2 Methods of Determination
In this experiment, you will learn to measure the plastic and liquid limit of a fine-grained soil and
classify it according to the BS1377 Soil Classification System. The details of the method are given in
the British Standards for laboratory soil testing BS1377. This standard is widely used in Singapore
soil testing practice and you should make an effort to familiarize yourself with it. There is a copy of
the BS1377 in the Central Library Reference Section as well as in the Geotechnical Laboratory. You
should go through the details of the test step-by-step as well as the forms used thoroughly to ensure
that you acquire good geotechnical testing practice.
2.2.1
Plastic Limit
In geotechnical testing, the plastic limit is defined as the minimum water content at which soil can be
deformed plastically. It is obtained by measuring the water content at which the soil can be rolled into
a thread 3 mm thick. In the experiment, approximately 20 g of the soil paste is moulded in the hand
until it dries sufficiently for slight cracks to appear. This start the soil paste off at a water content
which is often higher than the plastic limit (this is quite easily discerned from the strength and ductility
of the soil, with some experience). The sample is then divided into two approximately equal (10g)
portions and each of these is divided into four sub-samples. One of the sub-samples is taken and
rolled into a ball and then it is rolled over a glass sheet or some smooth surface using the open palm
of a hand to form a thread of soil (see Figure 1). If the soil can be thinned down to a thread of less
than 3mm diameter, the water content is higher than the plastic limit. In this event, the soil is
re-formed into a ball; and then re-rolled on the glass sheet. (This in effect reduces moisture content).
This process allows the heat from the hands to dry up the soil gradually, while the kneading keeps
the moisture content uniform throughout the sample. By alternately kneading (drying) and rolling
(testing) the soil, a point will be reached at which cracks will start to appear in the soil thread just as
it thins down to about 3mm. The water content of the soil at this point is measured and taken to be
plastic limit. At water content < PL, remoulding of specimen will cause soil to crack and crumble.
Shear strength of soil at PL 200 kPa. The same procedure is carried out on the other three
sub-samples, and other 10g portions.
6
Liquid Limit
The BS1377 recognizes two methods of determining the liquid limit. The first is the cone penetration
method, which is also the preferred method. The second method is the Casagrande method. In this
course, we will only deal with the cone penetration method, which has been proven to be much more
reliable. The principle of this method consists of allowing a cone of apex angle 30 and 80gm weight
to penetrate into a fixed volume of soil, which is contained within a standard aluminium cup. The
liquid limit is defined as the water content at which the penetrometer penetrates 20mm into the soil
when allowed to fall from a position of point contact with the soil surface.
The liquid limit is usually conducted on a portion of soil passing 425 m mesh. The soil is thoroughly
mixed with distilled water into a smooth thick paste, and stored in an airtight container for 24 hours
to allow for full penetration of the water.At the time of testing, the soil is remixed for 10 minutes to a
uniform water content which is less than the liquid limit (again, you can quite easily tell that this is so
from practice) and a portion of it is placed in the standard cup [taking care not to trap air within the
soil mass]. The soil surface is then levelled off with the top of the cup. Placing the cup on the stand,
lower the cone so that it just touches and marks the surface of the soil paste. The dial gauge is then
set and reading noted. The cone is released to penetrate the soil paste for exactly 5 seconds and
relocked in its new position. A second dial gauge reading in now taken. The difference between the
first and second dial readings gives the amount of cone penetration in mm. BS1377 requires each
water content to be penetration-tested twice and the penetration compared to ensure that they agree
within a specified tolerance. If the agreement is close, the water content of the soil paste is measured.
Otherwise the result is discarded and the test is repeated. If the penetration is less than 20mm, more
water is then added and the soil is remixed and re-tested. At least four different water contents, with
penetrations enveloping the 20mm mark, should be tested to give four points which are then plotted
on a graph of water content against penetration. A straight line is then fitted to the four points and the
water content at which the penetration is 20mm is then read off the graph.
7
Experimental Requirements
Each group will be given sufficient soil for the conduct of Atterberg limits tests. Determine the
Atterberg limits using the procedures outlined above and detailed in BS1377. Following the
procedures outlined above and detailed in BS1377, complete the appropriate forms given in these
appendices and determine the PL and LL. Note, in particular, that for the determination of LL, the
cone penetration test should be performed at least four times using the same sample with
gradual increase in water content. The amount of water added shall be chosen so that a
range of penetration values of about 15 mm to 25 mm is covered. Using the Atterberg limits
obtained from your experiment. Classify the soil according to the BS1377 soil classification system.
3. Compression and Consolidation of Soils
pc
10
C
Q
S
D
Cc = 0.007(LL-10%)
(5)
Undisturbed soil:
Cc = 0.009(LL-10%)
(6)
11
Schofield and Wroth (1968) proposes several semi-empirical relations based on the critical state
concept, including the following:
Cc = 0.01346PI
(7)
Cc = 0.02116(PL - 9%)
(8)
Cc = 0.00828(LL - 9%)
(9)
Wood also proposes the following semi-empirical relations based on the critical state concept:
Cc = 0.05Gs PI
(10)
in which Gs is the specific gravity of the soil solid, usually taken to be about 2.65. Based on local
experience so far, most, if not all, of the above relations appear to give an over-estimation of Cc
when compared to consolidation test results but Eq. 5 appears to give the best prediction. All these
relations can be used to correlate your Cc values from consolidation tests to your LL and PL values.
3.2 Rate of Consolidation
In many fine-grained soils, compression of the soil under loading is not instantaneous. This is
because, for the soil skeleton to compress, pore water has to be expelled. The theory of
consolidation will be discussed in detail in your lectures. The objective of the following sections is to
give you a basic level of understanding, mainly from a physical, rather than mathematical, viewpoint.
Consider the specimen of soil in your oedometer when it is subjected to a sudden increment in stress,
such as that applied by you when you increase the weights. The soil specimen consists of two
phases, viz. soil skeleton and pore water. You can think of the soil skeleton as behaving somewhat
like a sponge; in this case, the sponge is completely saturated with water. When you increase in
the load on the load hanger, the soil specimen will try to deform by compressing vertically and
expanding laterally. But lateral expansion is not possible since the soil specimen is constrained by a
stiff metallic ring. In such a condition, the only way for the soil specimen to settle is to undergo a
volumetric contraction. Since the specimen is completely saturated, water must be expelled from the
soil skeleton (or sponge) if the latter is contract volumetrically. If the soil skeleton (or sponge) is
highly impermeable, water will take a long time to flow out of the soil skeleton. In the short-term,
excess pore pressure will be generated which supports the load. The process of gradual timedependent settlement and pore pressure dissipation of the specimen under loading is known as
consolidation. In the classical consolidation process under increase in loading, the excess pore
pressure generally decreases whereas the settlement and effective stress increase with time. For low
permeability soils, this can take a long time. In such cases, not only is the final compression
important, but so too is the rate of consolidation. The parameter which is often used to describe the
rate of consolidation is the coefficient of consolidation cv.
In theory, cv can be deduced from the relationship
cv = k/(w mv)
(11)
However, in practice, this is often difficult since it is often difficult to determine k in the laboratory
reliably. Hence, this relationship should be used only as a last resort and also perhaps as a check.
The coefficient of consolidation can also be measured using the same oedometer or consolidation
test set-up in Fig. 1; indeed this is the normal way of determining cv. In order to determine the
12
coefficient of consolidation, settlement readings must taken at various times after load application;
this is different from the compression parameters Cc and Cs, which only requires the final settlement
to be measured after each loading increment. There are several different methods for determining the
coefficient of consolidation. However, probably the most commonly used method is Taylors
settlement-root-time method and Casagrandes log-time fitting method, which involves plotting
settlement (on the y-axis) against square root time of time (on the x-axis). The procedures for these
methods are given below.
3.2.1
Real consolidation events are often coloured by two other features, namely:
(a) Immediate settlement. When the load is first put on, a certain amount of acceleration occurs very
rapidly. This arises from small amounts of air being compressed in the sample and in the spaces
between the sample and the end platens. Thus the real settlement curve may contain a portion,
which is very steep (almost vertical), representing a rapid increase in settlement (see figure
above). To correct, it is usual to project the straight line portion backwards until it intersects the
settlement axis at the corrected zero. This point is then taken to be real origin of the settlement
curve, i.e. the initial origin is disregarded.
(b) Secondary compression. In our consolidation theory, we have assumed that the soil skeleton is
linearly elastic and that the time-dependent settlement during consolidation arises entirely from
the gradual flow of pore water to the outside of the sample. In reality, it is often not so. In
particular, the soil skeleton can exhibit creep behaviour (i.e. compression under a state of
constant effective stress) due to the chemical activity of clay particles. This phenomenon is
particularly significant in active soils such as marine clay and peat. To distinguish the creep
phenomenon of the soil skeleton from the classical consolidation, the former is known as
secondary compression/consolidation whilst the latter is often known as primary consolidation.
In the consolidation curve, secondary consolidation is manifested in a departure from the
classical consolidation curve towards the end of primary consolidation, in such a manner that the
actual consolidation curve does not tail off (see figure below).
The presence of secondary compression therefore presents problem for the estimation of final
settlement. Furthermore, since we know that secondary compression is significant at the tail end of
primary consolidation, we should try to avoid making use of the tail end of the consolidation curve to
estimate cv.
The Taylors root-time procedure is as follows (Figure 6):
1. Plot settlement vs time.
2. Draw a straight line (say OG) that coincides with the initial linear portion of the consolidation
curve.
3. Draw another straight line (say OC) through the corrected origin which has an inverse gradient
1.15 times that of line OG.
13
4. The point of intersection of line OC and the consolidation curve gives the point (t90, 90). Thus
t90 can be obtained by squaring the abscissa of the point of intersection, and cv obtained using the
relation cv = 0.848H2/t90.
C
Figure 6. Taylors root-time curve fitting procedure.
3.2.2
It has been observed that secondary compression, like most creep phenomenon, increases linearly
with the log10 of time. Figure 7 shows a typical settlement vs lg (time). In this curve, the secondary
compression appears as a straight line. The end of primary consolidation U = 1, is now identifiable
(approximately) by the break in the slope between the primary phase and the secondary phase,
thereby allowing us to find the final settlement . The point (lg(t50), 0.5) corresponding to 50%
consolidation (i.e. when the settlement reaches half of its final value) can be found by locating the
point on the consolidation curve with ordinate of 0.5. Hence, we can determine t50. We know
that at
U = 0.5, T = 0.196 = cv t50/H2. Therefore cv = 0.196H2/t50. Thus, knowing t50, cv can be found.
14
overburden stress to 100kPa by adding weights to the loading hanger. Repeat this sequence
over the next four days so as to subject the sample to the following overburden stresses:
DAY
OVERBURDEN STRESS (kPa)
1
50
2
100
3
200
4
400
5
100
6
Download final readings and wash up.
3.4 Data Processing
(1) Determine the initial water content of the sample used in the consolidation test and complete the
attached test header form.
(3) Plot the void ratio against effective pressure on a linear scale and determine the coefficient of
volume change mv at different effective pressures.
(4) Plot the void ratio against the log10 of the effective pressure and determine Cc, Cs and the precompression pressure pc.
(5) For each load increment, plot the settlement against the logarithm of time and thus determine the
cv values for each increment.
(6) By combining cv and mv in each increment, deduce the value of k for each increment. Comment
on the trend of increase or decrease of k with effective pressure.
(7) Compare your measured Cc values with the given correlations.
(8) Assess the reliability of your results and recommend design values for Cc, Cs, mv, cv and k.
16
Annex A
Form2.C
Location
Job ref.
Borehole/
Pit no.
Soil description
Sample no.
Depth
Test method
PLASTIC LIMIT
Container no.
Mass of wet soil + container
Mass of dry soil + container
Mass of container
Mass of moisture
Mass of dry soil
Moisture content
LIQUID LIMIT
Initial dial gauge reading
Final dial gauge reading
Cone Penetration
Average penetration
Container no.
Mass of wet soil + container
Mass of dry soil + container
Mass of container
Mass of moisture
Mass of dry soil
Moisture content
Average moisture content
Test no.
Test no.
mm
mm
mm
mm
g
g
g
g
g
%
%
Sample preparation *
as received
washed on 425 um sieve
air dried at ...........Deg C
oven dried at ........Deg C
not known
Proportioned retained
on 425 um sieve .......% %
Liquid limit :
%
25
20
15
10
Plastic limit :
Plasticity index :
* Delete as appropriate
30
40
Average
g
g
g
g
g
%
LIquid Limit
Cone Penetration mm
Date :
50
60
Moisture Content %
70
80
Operator
CheckedApproved
Annex B
WATER CONTENT / BULK DENSITY
Site
:
Bore Hole :
Sample No :
Natural / After
Consolidation / Direct Shear/
Vane Shear/Triaxial Shear /Test
Specimen Test No :
1
Date :
Can No.
Can only
Ring only
Water
Dry soil
gm
gm
gm
Water content %
gm
gm
Volume of soil
cm3
Bulk density
gm/cc
Natural / After
Consolidation / Direct Shear/
Vane Shear/Triaxial Shear /Test
Specimen Test No :
1
Date :
Can No.
Can only
Ring only
Water
Dry soil
gm
gm
gm
Water content %
gm
gm
Volume of soil
cm3
Bulk density
gm/cc
Annex C
Job ref.
Borehole/
Pit no.
Soil description
Sample no.
Depth
Date :
Test method
Machine no.
Cell no.
Ring no.
Height Ho
=
He ight of Solids=Hs
Initial Void ratio eo
=
=
Void Ratio
Increment No
0
1
2
3
4
5
20
mm
mm
(for fully saturated soil)
W x Gs
Pressure Cummulative
P kPa
compression
mm
Consolidated
height Ht mm
Void
Ratio e
Compressibility
Incremental Pressure
Height
Change
change dH DP kPa
mm
Height H0
mm
Where
Cv
e
mv
k
=
=
=
=
Mv
m2/kN
Consolidation
H
Cv
mm
m2/yr
k
10-10
m/s