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3.1 Manual For Laboratory Investigation PDF
3.1 Manual For Laboratory Investigation PDF
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FIELD IDENTIFICATION TEST
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1.1 Introduction
The identification is based on Visual- examination and manual test. The first step in any geotechnical
engineering project is to identify and describe the subsoil condition. For example, as soon as a ground is
identified as gravel, engineer can immediately form some ideas on the nature of problems that might be
encountered in a tunneling project. In contrast, a soft clay ground is expected to lead to other types of
design and construction considerations. Therefore, it is useful to have a systematic procedure for
identification of soils even in the planning stages of a project. Soils can be classified into two general
categories: (1) coarse grained soils and (2) fine grained soils. Usually coarse-grained soils are sand,
gravel, cobble and boulder, while fine-grained soils are silt and clay.
1.4 Apparatus
Spatula
Wooden hammer
Beaker
Glass rod / Stirrer
1/8inch diameter steel rod
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Boulder 12 in. (305 mm) or more Larger than basketball
Cobbles 3 in (76 mm) -12 in (305 mm) Grapefruit
Coarse Gravel % in. (19 mm) — 3 in. (76 mm) Orange or Lemon
Fine Gravel 4.75 mm (No.4 Sieve) — % in. (19 mm) Grape or Pea
*Particles finer than fine sand cannot be discerned with the naked eye at a distance of 8 in (20 cm).
If the major soil constituent is sand or gravel: Identify particle distribution. Describe as well
graded or poorly graded. Well-graded soil consists of particle sizes over a wide range.
Poorly graded soil consists of particles which are all about the same size. Identify particle
shape (angular, sub-angular, rounded, sub-rounded) using Figure 1.2 and Table 1.2.
According to USCS followed by USBR (USA), Army Corps of Engineers ASTM and ASCE:
Range of silt size is 0.002 mm to 0.074 mm and clay particles are smaller than 0.002 mm. (After
S.K.–Soil Mechanics and Foundation Engineering, Sixth Revised Edn. 2005, p. 17)
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If the gravel fraction is greater than sand fraction, identify the soil as "gravel" (G). The gravel fraction
may be further divided into
coarse gravel (75 mm-20 mm) and
fine gravel (20 mm-4.75 mm).
If the gravel fraction is equal to or less than sand fraction, identify the soil as "sand" (S). The sand
fraction may be further divided into
Coarse sand (4.75 mm – 2 mm),
Medium sand (2 mm – 425 microns), and
Fine sand (425 microns – 75 microns)
Identify the soil further as ―clean gravel‖ or "clean sand" if the percentage of fines is estimated to be
less than 5 percent. Identify it as "gravel with fines" or "sand with fines" if the percentage of fines is
estimated to be more than 15%.
Classify the "clean gravels" or "clean sand" as follows:
Identify the soil as well graded gravel (GW), or as a well graded sand (SW) if there is good
representation of all particle sizes.
Identify the soil as poorly graded gravel (GP), or as a poorly graded sand (SP) if it contains
predominantly of one size (uniformly graded) or it has a wide range of sizes with some
intermediate size(s) obviously missing (gap graded).
1. Classify "gravel with fines" or "sand with fines" as follows: If the other course grained constituent
is less than 15% then:
Silty gravel (GM) or silty sand (SM) if the fines have little or no plasticity, or
Clayey gravel (GC) or clayey sand (SC), if the fines are of low to medium or high plasticity.
If the other course grain constituent is greater than 15%, then the group name shall be a
combination from the two columns below:
2. If the percentage of fine is in between 5~15% then the group name shall be a combination from
the two columns below:
Boundary classifications: Assume the coarser soil first, when there is a choice, complete the
classification and assign the appropriate symbol Then beginning where the choice was made, assume
the finer soil, complete the classification and assign the second group symbol. The examples are as
follows: GW-GP, GM-GC, GW-GM, GW-GC, SW-SP, SM-SC, SW-SM, SW-SC, GW-SW, GP-SP, GM-
SM, GC-SC, SM-ML, SC-CL etc.
Dispersion Test.
Dry strength Test.
Dilatancy Test/Shaking Test/Water Mobility Test.
Plasticity Test/Toughness Test.
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1.1.1 Dispersion Test:
A small quantity of the collected soil sample is dispersed or mixed with water in a glass
cylinder or test tube or beaker and then allowed to settle.
Silt particles usually settle in 15 to 60 min. whereas clay particles will remain in suspension for at least
several hours or may remain even for several days. If some sand particles are present in sample, then it
settles in 30 to 60 sec.
At first the soil samples are molded. Then prepare four or five pats from this molded sample,
about 25 mm in diameter and 6 mm in thickness.
Dry all the pats completely (either naturally or in an oven).
Measure its resistance to crushing between the fingers. This resistance, called the dry strength or
crushing strength, is a measure of the plasticity of the soil.
Crushing of dry clay lumps is relatively difficult, whereas silt lumps break quite easily.
Test the strength of the dry pats or lumps by crushing between the fingers and note the
strength in accordance with the criteria in Table 1.3.
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Figure 1-3:Dry Strength Test
Table 1.2: Dry Strength Test (Engineering Properties of Soils Based on Laboratory Testing Prof.
Krishna Reddy, UIC)
Description Criteria
None The dry specimen crumbles into powder with mere pressure of handling
Low The dry specimen crumbles into powder with some finger pressure
Medium The dry specimen break into pieces or crumbles with considerable finger pressure
High The specimen cannot be broken with finger pressure. Specimen will break into pieces
between thumb and hand surface
Very H i g h The specimen cannot be broken between the thumb and hard surface
The presence of high-strength water soluble cementing materials, such as calcium carbonates, may
cause exceptionally high dry strength. The presence of calcium carbonate can usually be deleted from
the intensity of the reaction with dilute hydrochloric acid.
Description Criteria
None No visible change in specimen
Water appears slowly on the surface of the specimen during shaking and does not disappear or disappear
Slow
slowly upon squeezing
Water appears quickly on the surface of the specimen during shaking and disappears quickly upon
Rapid
squeezing
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1.1.4 Toughness or plasticity Test:
Following the completion of the dilatancy test, the test specimen is shaped into an elongated pat and
rolled by hand on a smooth surface or between the palms into a thread about 1/8 in, in diameter. If the
sample is too wet to roll easily, it should be spread into a thin layer and allowed to lose some water by
evaporation.
Fold the sample threads and reroll repeatedly until the thread crumbles at a diameter of about 1/8 in.
The thread will crumble at a diameter of 1/8 in, when the soil is near the plastic limit. Note the pressure
required to roll the thread near the plastic limit.
Also note the strength of the thread. After the thread crumbles, note the toughness of the
materials during kneading.
In a word, it is expressed as: clay can be rolled out into small threads (about 1/8in. thickness), whereas
silt is much more difficult to roll into small threads and generally requires more water.
Description Criteria
Low Only slight pressure is required to roll the tread near the plastic limit. The thread and
the lump are weak and soft.
Medium Medium pressure is required to roll the tread near the plastic limit. The thread and the
lump have medium stiffness.
High Considerable pressure is required to roll the thread near the plastic limit. The thread
and the lump have very high stiffness.
Table 1.5: Plasticity Test (Engineering Properties of Soils Based on Laboratory Testing Prof. Krishna Reddy,
UIC)
Description Criteria
Non plastic A 1/8 in, thread cannot be rolled at any water content.
Low The thread can barely be rolled and the lump cannot be formed when drier than the plastic limit.
Medium The thread is easily to roll and not much time is required to reach the plastic limit. The thread
cannot be rolled after reaching the plastic limit. The lump crumbles when drier than the plastic
limit.
High It takes considerable time rolling and kneading to reach the plastic limit. The thread can be rolled
several times after reaching the plastic limit. The lump can be formed without crumbling when drier
than the plastic limit.
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Table 1.6: : Field Identification of Fine Grained Soil (Engineering Properties of Soils Based on
Laboratory Testing Prof. Krishna Reddy, UIC)
Table 1.7: Identification of inorganic fine-grained soil (Engineering Properties of Soils Based on
Laboratory Testing Prof. Krishna Reddy, UIC)
Table 1.8: Criteria for describing soil-moisture condition (Engineering Properties of Soils
Based on Laboratory Testing Prof. Krishna Reddy, UIC)
Description Criteria
Dry Soil is dry to the touch, dusty, a clear absence of moisture
Moist Soil is damp, slight moisture ;soil may begin to retain molded form
Wet Soil is clearly wet; water is visible when sample is squeezed
Saturated Water is easily visible and drains freely from the sample
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MOISTURE CONTENT DETERMINATION
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2.1 Introduction
The water content is the ratio, expressed as a percentage, of the mass of pore or free water in a given mass of
soil to the mass of the dry soil solids. For many soils, the water content may be an extremely important index
used for establishing the relationship between the way a soil behaves and its properties. The consistency
of a fine-grained soil largely depends on its water content. The water content is also used in expressing
the phase relationships of air, water, and solids in a given volume of soil.
2.4 Apparatus
3. Drying Oven
4. Balance
5. Specimen Container
6. Gloves
7. Spatula
2.6 Calculation
(1) Determine the mass of soil solids.
MS = M3-M1
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(2) Determine the mass of water.
MW=M2-M3
= 100%
Sample No 1 2 3
Wt. of the dry can (M1),g 10.0
Wt. of Moist soil + can, (M2),g 35.0
Wt. of dry soil + can, (M3),g 28.0
Wt. of water (Ms),g 7.0
Wt. of solid (Ms),g 18.0
Moisture Content, % 38.89
Sample Calculation-
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Specific Gravity Test
3.1 Introduction
Specific gravity is the ratio of unit weight of soil at a stated temperature to the unit weight of same volume of gas-
free distilled water at the stated temperature. In general, the specific gravity Gs of a material represents the
ratio of the mass of a given volume of that material at a temperature to the mass of an equal volume of
distilled water at the same temperature. It is usually determined by the principle of displacement of water
by soil in a pycnometer.
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3.3 Standard References
ASTM D 854-00 – Standard Test for Specific Gravity of Soil Solids by Water Pycnometer.
3.4 Apparatus
13. Pycnometer (volumetric bottle)
14. Balance (0.01g sensitivity)
15. Distilled water,
16. Drying oven,
17. Desiccator,
18. Vacuum source (optional),
19. Funnel,
20. Thermometer,
21. Pipette or medicine dropper,
22. Spoon etc.
3.6 Calculation
The specific gravity of the soil, GT,
=
+
( ) °
=
( ) 20°
3.7 Result
1. Identification of the soil (material) being tested, such as boring number, sample number, depth,
and test number.
2. Visual classification of the soil being tested (group name and symbol in accordance with Practice
D 2487).
3. Percent of soil particles passing the No. 4 (4.75-mm) sieve.
4. If any soil or material was excluded from the test specimen, describe the excluded material.
Client:
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Determination no 1 2 3
Wt. of bottle (gm) 96.20
Wt. of bottle + dry soil (gm) 146.30
Wt. of dry soil, Ws (gm) 50.10
Wt. of bottle + water + soil, W1 (gm) 376.50
Wt. of bottle + water. W2 (gm) 344.51
Room Temperature, T C 27
Specific gravity of water, (Gw) at T C 0.9982
Specific gravity of water, (Gw) at 20 C 0.9965
Specific gravity of soil at 20 C 2.77
Sample Calculation:
50.1
= = 2.77
50.1 376.5 + 344.51
0.9982
= 2.77 × = 2.774
0.9965
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Standard Test Methods for Amount of Material in Soils
Finer than the No. 200 (75-μm) Sieve
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4.1 Introduction
These test methods cover determination of the amount of material finer than a 75-μm (No. 200) sieve by
washing. This test identifies soil as coarse grained or fine grained.
4.4 Apparatus
Balance—A balance or scale conforming to the requirements of Specification D 4753, readable
(with no estimation) to 0.1 % of the test mass, or better.
Sieves—A minimum nest of two sieves is recommended, the lower must be a 75-μm (No. 200)
sieve and the upper may be a 425-μm (No. 40) or larger sieve. Chose a sieve with a diameter
sufficient to handle the size of specimen. The 75-μm sieve should have a backing to prevent
damage.
Oven—An oven of sufficient size, capable of maintaining a uniform temperature of 100 °C
(230°F)
4.6 Calculation
Calculate the amount of material passing the 75-μm (No. 200) sieve by washing using the following
formula:
= × 100%
Where, A = percentage of material finer than the 75-μm sieve by washing, nearest 0.1 %
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C = dry mass of specimen retained on the 75-μm sieve including the amount retained on an upper sieve
after washing, gm.
4.7 Result
1. Report the percentage of material finer than the 75-μm (No. 200) sieve by washing to the nearest
0.1 %.
2. Indicate whether the specimen was soaked and length of time.
3. Indicate method used (A or B).
Weight of
Weight Weight of
Weight Weight of Can + Percentage Percentage of
Serial Depth Can of Dry Washed
of Can Can + Dry Washed of Fines Coarse
No. (m) No. Soil Dry Soil
(gm) Soil (gm) Dry Soil Content (%) Content (%)
(gm) (gm)
(gm)
Sample Calculation-
Here,
B= 63.58 gm
C= 19.72 gm
A= ((63.58-19.72)/63.58) *100%
= 69 %
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Grain Size Analysis (Sieve Analysis)
5.1 Introduction
Sieve analysis is performed to determine the gradation of different particle sizes of coarse grained soil or
coarser portion of a soil containing both coarse (sand & silt) and fine (silt & clay) particles. A sieve analysis
consists of shaking the soil through a stack of wire screens with openings of known sizes; the definition
of particle diameter for a sieve test is therefore the side dimension of a square hole. It should be noted
that sieve analysis does not give any idea about the shape of the particles. Sieves are made of woven
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wires with square openings. From sieve analysis, information about grain size distribution is obtained.
Besides the gradation curve, other parameters namely uniformity coefficient Cu, coefficient of curvature,
Cc are determined and all this information are used for classification.FM (Fineness Modulus) is
determined from sieve analysis done on fine and coarse aggregates. However, FM has almost no
meaning and use in geotechnical interpretation and understanding of soil behavior as a foundation
material.
5.4 Apparatus
26. ASTM Sieve #4, #8, #16, #30, #50, #100, #200 Pan
27. Lead
28. Brush
29. Container
30. Spoon
31. Bowel
32. Balance
33. Sieve shaker
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12 1.70 80 0.180
14 1.40 100 0.150
16 1.18 120 0.125
18 1.00 140 0.106
20 0.85 200 0.075
25 0.71 270 0.053
30 0.60 400 0.0381
5.6 Calculation
1. Obtain the mass of soil retained on each sieve by subtracting the weight of the empty sieve from
the mass of the sieve + retained soil, and record this mass as the weight retained on the data
sheet. The sum of these retained masses should be approximately equals the initial mass of the
soil sample. A loss of more than two percent is unsatisfactory.
2. Calculate the percent retained on each sieve by dividing the weight retained on each sieve by
the original sample mass.
3. Calculate the percent passing (or percent finer) by starting with 100 percent and subtracting the
percent retained on each sieve as a cumulative procedure.
4. Calculate Fineness Modulus.
∑( )
. =
100
5. Make a semi logarithmic plot of grain size vs. percent finer.
6. Find the value of D10, D30 & D60
7. Compute Uniformity coefficient, Cu and Coefficient of gradation, Cz for the soil.
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=
×
5.7 Results
The results of a grain size analysis are usually presented in the form of a distribution curve; this curve is
obtained by plotting diameter against per cent finer. The uniformity of a soil can be expressed by the
uniformity coefficient which is the ratio of D60 to D10. A soil having a uniformity coefficient smaller than
about 2 would be considered ‘uniform’.
There are several grain size classifications , which give good indications of typical particle sizes.
Client:
Sample Calculation-
Ws = W2-W1
=335.05-334.89
=0.16
= 100-0.16
=99.3 %
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SAND
Gravel
Coarse Medium Fine
100
90
80
70
Percent finer (%)
60
50
40
30
20
10
0
10 4.75 2 1 0.425 0.1 0.075 0.01
Particle Size (mm)
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6.1 Introduction
Grain size distribution of soil that contain significant amount of finer particles (silt and clay) cannot be
done by sieve analysis. Hydrometer analysis is required to determine the grain size distribution of the
finer portion. For many natural soils we require both sieve analysis and hydrometer analysis to obtain the
complete gradation of the coarse and fine fraction. In the sieve analysis test we have used #200 sieve
(opening 0.074 mm) as the finest sieve. Now hydrometer analysis will be performed on a fine grained soil
that passes #200 sieve.
According to ASTM D422, when combined analysis is required, the sample is to be divided into two parts.
Sieve analysis is to be done on the coarser portion and hydrometer analysis is to be done into finer
portion. Division of the sample into two portion is to be done by either of #4 (4.75mm), #10 (2.00 mm),
#40 (0.425mm) or #200 (0.074 mm) sieve depending on the specific gravity of particles. However, for our
natural soils separation on #200 sieve will be sufficient.
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6.2 Objective of the test
The lab test is performed to determine the percentage of different grain sizes contained within a
fine grained soil.
The hydrometer analysis is performed to determine the distribution of the finer particles.
6.4 Apparatus
Hydrometer
Glass measuring cylinder (jar), 1000ml
Rubber bung for the cylinder (jar)
Mechanical stirrer
Weighing balance, accuracy 0.01g
Oven
Deflocculating agent.
Desiccator
Evaporating dish
Conical flask or beaker, 1000ml
Stop watch
Wash bottle
Thermometer
Water bath
75 µ Sieve
Scale.
Where,
In which,
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K= constant
L= effective depth,
t= time in minutes at which observation is taken, reckoned with respect to the beginning of
sedimentation.
100 × ×
=
Where,
1. Take about 800ml of water in one measuring cylinder. Place the cylinder on a table and observe the
initial reading.
2. Immerse the hydrometer in the cylinder. Take the reading after the immersion.
3. Determine the volume of the hydrometer (VH) which is equal to the difference between the final and
initial readings. Alternatively weigh the hydrometer to the nearest 0.1g. The volume of the hydrometer
in ml is approximately equal to its mass in grams.
4. Determine the area of cross section (A) of the cylinder. It is equal to the volume indicated between any
two graduations divided by the distance between them. The distance is measured with an accurate
scale.
5. Measure the distance (H) between the neck and the bottom of the bulb. Record it as the height of the
bulb (h).
6. Measure the distance (H) between the neck to each marks on the hydrometer (Rh).
7. Determine the effective depth (L), corresponding to each of the mark (Rh) as
[Note: The factor VH/A should not be considered when the hydrometer is not taken out when taking
readings after the start of the sedimentation at ½, 1, 2, and 4 minutes.]
8. Draw a calibration curve between L and Rh. Alternatively, prepare a table between L and Rh. The curve
may be used for finding the effective depth L corresponding to reading Rh.
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Figure 6-1:Hydrometer Method
1. Insert the hydrometer in the measuring cylinder containing about 700ml of water.
2. Take the readings of the hydrometer at the top and at the bottom of the meniscus.
3. Determine the meniscus correction, which is equal to the difference between the two readings.
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4. The meniscus correction Cm is positive and is constant for the hydrometer.
5. The observed hydrometer reading Rh’ is corrected to obtain the corrected hydrometer reading Rh as
= +
1. Weigh accurately, to the nearest 0.01g about 50g air-dried soil sample passing 2mm IS sieve, obtained
by riffling from the air-dried sample passing 4.75mm IS sieve. Place the sample in a wide mouthed conical
flask.
2. Add about 150ml of hydrogen peroxide to the soil sample in the flask. Stir it gently with a glass rod for a
few minutes.
3. Cover the flask with a glass plate and leave it to stand overnight.
4. Heat the mixture in the conical flask gently after keeping it in an evaporating dish. Stir the contents
periodically. When vigorous frothing subsides, the reaction is complete. Reduce the volume to 50ml by
boiling. Stop heating and cool the contents.
5. If the soil contains insoluble calcium compounds, add about 50 ml of hydrochloric acid to the cooled
mixture. Stir the solution with a glass rod for a few minutes. Allow it to stand for one hour or so. The
solution would have an acid reaction to litmus when the treatment is complete.
6. Filter the mixture and wash it with warm water until the filtrate shows no acid reaction.
7. Transfer the damp soil on the filter and funnel to an evaporating dish using a jet of distilled water. Use
the minimum quantity of distilled water.
8. Place the evaporating dish and its contents in an oven and dry it at 105 to 110-degree Celsius. Transfer
the dish to a desiccator and allow it to cool.
9. Take the mass of the oven-dried soil after pretreatment and find the loss of mass due to pretreatment.
10. Add 100ml of sodium hexa-metaphosphate solution to the oven – dried soil in the evaporating dish after
pretreatment.
12. Transfer the mixture to the cup of a mechanical mixture. Use a jet of distilled water to wash all traces of
the soil out of the evaporating dish. Use about 150 ml of water. Stir the mixture for about 15minutes.
13. Transfer the soil suspension to a 75 µ IS sieve placed on a receiver (pan). Wash the soil on this sieve
using a jet of distilled water. Use about 500ml of water.
14. Transfer the soil suspension passing 75 µ sieve to a 1000ml measuring cylinder. Add more water to
make the volume exactly equal to 1000ml.
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15. Collect the material retained on 75 µ sieve. Dry it in an oven. Determine it’s mass. If required, do the
sieve analysis of this fraction.
1. Place the rubber bung on the open end of the measuring cylinder containing the soil suspension. Shake
it vigorously end-over-end to mix the suspension thoroughly.
2. Remove the bung after the shaking is complete. Place the measuring cylinder on the table and start the
stop watch.
3. Immerse the hydrometer gently to a depth slightly below the floating depth, and then allow it to float freely.
4. Take hydrometer reading (Rh’) after 1/2, 1, 2 and 4 minutes without removing the hydrometer from the
cylinder.
5. Take out the hydrometer from the cylinder, rinse it with distilled water.
6. Float the hydrometer in another cylinder containing only distilled water at the same temperature as that
of the test cylinder.
7. Take out the hydrometer from the distilled water cylinder and clean its stem. Insert it in the cylinder
containing suspension to take the reading at the total elapsed time interval of 8minutes. About 10 seconds
should be taken while taking the reading. Remove the hydrometer, rinse it and place it in the distilled
water after reading.
8. Repeat the step (7) to take readings at 15, 30, 60, 120 and 240minutes elapsed time interval.
9. After 240 minutes (4 hours) reading, take readings twice within 24 hours. Exact time of reading should
be noted.
10. Record the temperature of the suspension once during the first 15minutes and thereafter at the time of
every subsequent reading.
11. After the final reading, pour the suspension in an evaporating dish, dry it in an oven and find its dry
mass.
12. Determine the composite correction before the start of the test and also at 30min, 1, 2 and 4 hours.
Thereafter just after each reading, composite correction is determined.
13. For the determination of composite correction (C), insert the hydrometer in the comparison cylinder
containing 100ml of dispersing agent solution in 1000 ml of distilled water at the same temperature. Take
the reading corresponding to the top of meniscus. The negative of the reading is the composite correction.
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Figure 6-3: Downward Movement of Hydrometer
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Table 1: Observation recording sheet
1. Oven dry the collected disturbed sample and then break up all lumps with the grinding
machine or mechanically by hammer and fingers.
2. Run a sieve analysis as above. Then wash the soil retained on the No. 200 sieve.
3. Weigh out to 0.01g about 50g of the dry soil retained in the pan from the sieve analysis.
4. Run a hydrometer test on the dry soil following above procedure.
5. Compute the particle size and percent finer for the two parts of the combined analysis as
shown in sieve analysis and hydrometer analysis. The weight of dry soil, Ws to be used in
computing the sieve analysis should be the total sample.
6. The corrected percentage, N is found as follows:
= × = % . 200
Where,
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Atterberg Limit Test
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7.1 Introduction
In the early 1900’s Swedish soil scientist, A. Atterberg, identified different states in cohesive soils depending
on the amount of water in the system. After many experiments, Atterberg came to the realization that at least
two parameters were required to define plasticity of clays – the upper and lower limits of plasticity. He also
defined the plasticity index, which is the range of water content where the soil is plastic, and he was the first
to suggest that it could be used for soil classification. In present geotechnical engineering practice, we usually
use the Liquid Limit (LL or WL), the Plastic Limit (PL or WP), and sometimes the Shrinkage Limit (SL or
Ws).
He defined the LL as that water content at which a standard-groove cut in the remolded soil sample by a
grooving tool will close over a distance of 13 mm (1/2 in) at 25 blows of the LL cup falling 10 mm on a hard
rubber or micarta plastic base. In practice, it is difficult to mix the soil so that the groove closure occurs at
exactly 25 blows, but Casagrande found that if you plot the water contents of tests where you get closure at
other blow counts versus the logarithm of the number of blows, you get a straight line called the flow curve.
Where the flow curve crosses 25 blows, that water content is defined as the liquid limit.
The PL is defined as the water content at which a thread of soil just crumbles when it is carefully rolled out
to a diameter of 3 mm. It should break up into segments about 3 to 10 mm long. If the threads can be rolled
to a smaller diameter, then the soil is too wet (above the PL); if it crumbles before you reach 3mm in diameter,
then you are past the PL.
7.4 Apparatus
Liquid limit device
Porcelain (evaporating) dish
Flat grooving tool with gage,
Moisture cans
Balance
Glass plate
Spatula
Wash bottle filled with distilled water
Drying oven set at 1050 C.
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7.5 Liquid Limit
2. Weigh four of the empty moisture cans with their lids, and record the respective weights and can numbers
on the data sheet.
3. Adjust the liquid limit apparatus by checking the height of drop of the cup. The point on the cup that meets
the base should rise to a height of 10 mm. The block on the end of the grooving tool is 10 mm high and
should be used as a gage. Practice using the cup and determine the correct rate to rotate the crank so that
the cup drops approximately two times per second.
4. Place a portion of the previously mixed soil into the cup of the liquid limit apparatus at the point where the
cup rests on the base. Squeeze the soil down to eliminate air pockets and spread it into the cup to a depth
of about 10 mm at its deepest point. The soil pat should form an approximately horizontal surface.
5. Use the grooving tool carefully cut a clean straight groove down the center of the cup. The tool should
remain perpendicular to the surface of the cup as groove is being made. Use extreme care to prevent sliding
the soil relative to the surface of the cup.
6. Make sure that the base of the apparatus below the cup and the underside of the cup is clean of soil. Turn
the crank of the apparatus at a rate of approximately two drops per second and count the number of drops,
N, it takes to make the two halves of the soil pat come into contact at the bottom of the groove along a
distance of 13 mm (1/2 in.). If the number of drops exceeds 50, do not record the number of drops, otherwise,
record the number of drops on the data sheet.
7. Take a sample, using the spatula, from edge to edge of the soil pat. The sample should include the soil
on both sides of where the groove came into contact. Place the soil into a moisture can cover it. Immediately
weigh the moisture can be containing the soil, record its mass, remove the lid, and place the can into the
oven. Leave the moisture can in the oven for at least 16 hours. Place the soil remaining in the cup into the
porcelain dish. Clean and dry the cup on the apparatus and the grooving tool.
8. Remix the entire soil specimen in the porcelain dish. Add a small amount of distilled water to increase the
water content so that the number of drops required closing the groove decrease.
9. Repeat steps six, seven, and eight for at least two additional trials producing successively lower numbers
of drops to close the groove. One of the trials shall be for a closure requiring 25 to 35 drops, one for closure
between 20 and 30 drops, and one trial for a closure requiring 15 to 25 drops. Determine the water content
from each trial by using the same method used in the first laboratory. Remember to use the same balance
for all weighing.
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Figure 7-1:Liquid limit Test
Figure 7-2:(a) Grind the soil sample into pieces (b) Mix considerable amount of water with
the soil and make a paste (c) Using the spatula place soil sample to the liquid limit device, cut
the soil sample using grooving tools and give anti clockwise blow. (d) After come in contact
the soil take samples, weight and dry them.
37 | P a g e
7.5.2 Calculation to Determine Liquid Limit
1. Calculate the water content of each of the liquid limit moisture cans after they have been in the oven for
at least 16 hours.
2. Plot the number of drops, N, (on the log scale) versus the water content (w). Draw the best-fit straight line
through the plotted points and determine the liquid limit (LL) as the water content at 25 drops.
Client:
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Bore Hole No.: 162 Sample ID: D-01 Depth: 15.0 m
45
40
Moisture Content (%)
35
30
25
20
10 20 30 40 50
No. of Blows (N)
1. Weigh the remaining empty moisture cans with their lids, and record the respective weights and can
numbers on the data sheet.
2. Take the remaining 1/4 of the original soil sample and add distilled water until the soil is at a consistency
where it can be rolled without sticking to the hands.
3. Form the soil into an ellipsoidal mass. Roll the mass between the palm or the fingers and the glass plate.
Use sufficient pressure to roll the mass into a thread of uniform diameter by using about 90 strokes per
minute. (A stroke is one complete motion of the hand forward and back to the starting position.) The thread
shall be deformed so that its diameter reaches 3.2 mm (1/8 in.), taking no more than two minutes.
4. When the diameter of the thread reaches the correct diameter, break the thread into several pieces. Knead
and reform the pieces into ellipsoidal masses and re-roll them. Continue this alternate rolling, gathering
together, kneading and re-rolling until the thread crumbles under the pressure required for rolling and can
no longer be rolled into a 3.2 mm diameter thread.
5. Gather the portions of the crumbled thread together and place the soil into moisture can, and then cover
it. If the can does not contain at least 6 grams of soil, add soil to the can from the next trial. Immediately
weigh the moisture can be containing the soil, record it’s mass, remove the lid, and place the can into the
oven. Leave the moisture can in the oven for at least 16 hours.
6. Repeat steps three, four, and five at least two more times. Determine the water content from each trial by
using the same method used in the first laboratory. Remember to use the same balance for all weighing.
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Figure 7-4: (a) Ellipsoidal Soil Mass (b) Soil Rolling (c) Soil Gets Crumbled at 1/8 inch
2. Compute the average of the water contents to determine the plastic limit, PL. Check to see if the difference
between the water contents is greater than the acceptable range of two results (2.6 %).
3. Calculate the plasticity index, PI=LL-PL. Report the liquid limit, plastic limit, and plasticity
index to the nearest whole number, omitting the percent designation.
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Wt. of moisture, Ww= W2 – W3 = 19.72 -16.63 = 3.09 gm
2. Coat the inside of the shrinkage dish with a thin layer of petroleum jelly, silicone grease, or similar lubricant
to prevent the adhesion of the soil to the dish.
3. Determine and record the mass in grams of the empty dish, MT.
4. Place the shrinkage dish in the shallow pan in order to catch any mercury overflow.
6. Remove the excess mercury by pressing the glass plate firmly over the top of the shrinkage dish.
7. Determine the volume of mercury held in the shrinkage dish either by means of the glass graduate or by
dividing the measured mass of mercury by the mass density of mercury (equal to 13.55 Mg/m3).
3. Remove the excess mercury by pressing the glass plate with the three prongs firmly over
the top of the cup.
4. Place the evaporating dish in the shallow pan in order to catch any mercury overflow.
Place the cup filled with mercury in the evaporating dish and rest the soil pat on the
surface of the mercury (it will float).
41 | P a g e
5. Using the glass plate with the three prongs gently press the pat under the mercury and
press the plate firmly over the top of the cup to expel any excess mercury. Observe that
there is no air trapped between the plate and mercury,
6. Measure the volume of the mercury displaced into the evaporating dish either by means
of the glass graduate or by dividing the measured mass of mercury by the mass density of
mercury.
( )
= × 100
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UNCONFINED COMPRESSION TEST
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8.1 Introduction
For soils, the undrained shear strength (Su) is necessary for the determination of the bearing capacity of
foundations, dams, etc. The undrained shear strength (Su) of clays is commonly determined from an
unconfined compression test. The undrained shear strength (Su) of a cohesive soil is equal to one half the
unconfined compressive strength (qu) when the soil is under the f = 0 condition (= the angle of internal
friction). The most critical condition for the soil usually occurs immediately after construction, which
represents undrained conditions, when the undrained shear strength is basically equal to the cohesion (c).
8.4 Apparatus
Compression device
Load and deformation dial gauges
Sample trimming equipment
Balance
Moisture can.
, ∈=
44 | P a g e
6. Carefully place the specimen in the compression device and center it on the bottom plate. Adjust
the device so that the upper plate just makes contact with the specimen and set the load and
deformation dials to zero.
7. Apply the load so that the device produces an axial strain at a rate of 0.5% to 2.0% per minute, and
then record the load and deformation dial readings on the data sheet at every 20 to 50 divisions on
deformation the dial.
8. Keep applying the load until (1) the load (load dial) decreases on the specimen significantly, (2) the
load holds constant for at least four deformation dial readings, or (3) the deformation is significantly
past the 15% strain that was determined in step 5.
9. Draw a sketch to depict the sample failure.
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8.6 Calculation
1. Convert the dial readings to the appropriate load and length units, and enter these values on the
data sheet in the deformation and total load columns. (Confirm that the conversion is done correctly,
particularly proving dial gage readings conversion into load).
2. Compute the sample cross-sectional area
= ×
4
3. Compute the strain,
, ∈=
=
1 ∈
5. Using Ac, compute the specimen stress,
8.7 Result
The results of an unconfined test can be presented in a summary table and/or by a stress-strain curve. An
indication of typical values of shear strength is given by the following classification of clay based on
consistency:
BH No:
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Sample No:
Can No:
Weight of Can =
Weight of sample=
Weight of water =
Moisture Content =
Sample Calculation-
47 | P a g e
.
Stress, σ= = .
= 0.000
280
240
Axial Stress (kN/m2)
200
160
120
115.2
80
40
0
0.0 2.0 4.0 6.0
5.91 8.0 10.0 12.0 14.0 16.0
Axial Strain (%)
Unconfined Compressive Strength, qu = 115.2 kN/m2
Axial Strain at Failure = 5.91 %
Moisture Content = 20.74 % Checked by
Wet Unit Weight = 18.2 kN/m3
Dry Unit Weight = 15.1 kN/m3
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Direct Shear Test
49 | P a g e
9.1 Introduction
The shear strength is one of the most important engineering properties of a soil, because it is required
whenever a structure is dependent on the soil’s shearing resistance. The shear strength is needed for
engineering situations such as determining the stability of slopes or cuts, finding the bearing capacity for
foundations, and calculating the pressure exerted by a soil on a retaining wall. The direct shear test is one
of the oldest strength tests for soils. In this laboratory, a direct shear device will be used to determine the
shear strength of a cohesion less soil (i.e. angle of internal friction (). From the plot of the shear stress
versus the horizontal displacement, the maximum shear stress is obtained for a specific vertical confining
stress.
9.4 Apparatus
Direct shear device,
Load and deformation dial gauges,
Balance.
2. Measure the diameter and height of the shear box. Compute 15% of the diameter in millimeters.
50 | P a g e
3. Carefully assemble the shear box and place it in the direct shear device. Then place a porous stone and
a filter paper in the shear box.
4. Place the sand into the shear box and level off the top. Place a filter paper, a porous stone, and a top
plate (with ball) on top of the sand.
5. Remove the large alignment screws from the shear box. Open the gap between the shear box halves to
approximately 0.025 in. using the gap screws, and then back out the gap screws.
6. Weigh the pan of soil again and compute the mass of soil used.
7. Complete the assembly of the direct shear device and initialize the three gauges (Horizontal
displacement gage, vertical displacement gage and shear load gage) to zero.
8. Set the vertical load (or pressure) to a predetermined value, and then close bleeder valve and apply the
load to the soil specimen by raising the toggles witch.
9. Start the motor with selected speed so that the rate of shearing is at as elected constant rate, and take
the horizontal displacement gauge, vertical displacement gage and shear load gage readings. Record the
readings on the data sheet. (Note: Record the vertical displacement gage readings, if needed).
10. Continue taking readings until the horizontal shear load peaks and then falls, or the horizontal
displacement reaches 15% of the diameter.
9.6 Calculation
7. Calculate the density of the soil sample from the mass of soil and volume of the shear box.
8. Convert the dial readings to the appropriate length and load units and enter the values on the data
sheet in the correct locations. Compute the sample area A, and the vertical (Normal) stress σ,
9. Calculate shear stress () using F/A ,Where F = shear force measured with shear load gage.
10. Plot the shear stress () versus shear displacement.
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Figure 9-2:Stress vs Displacement Graph
11. Calculate the maximum shear stress for each test.
12. Plot the value of the maximum shear stress versus the corresponding vertical stress for each test,
and determine the angle of internal friction () from the slope of the approximated Mohr-Coulomb
failure envelope.
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9.7 Result
A typical value of ф is approximately 30 .
BH No:
Sample No:
Initial Diameter, D =
Initial Length, L =
Area, A=
Volume, V=
Can No:
Weight of Can =
Weight of sample=
Weight of water =
Moisture Content =
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: 10.00
IDR: 512 FDR: 501.5 Weight, P Time (min): 23
Kg
54 | P a g e
9.9 Sample Graph
200187.0
Shear Stress (kN/m2)
150
100.2
100
64.0
0
0.00 2.00 4.00 6.00 8.00 10.00 12.00
Horizontal Displacement (mm)
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Bore Hole No.: 01 Sample No.: D-06 Sample Depth: 9.0 m
200
y = 1.031x + 20.667
180
160
140
Shear Stress (kN/m2)
120
100
80
60
40
20
0
0 20 40 60 80 100 120 140 160 180
Effective Normal Stress (kN/m2)
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Consolidation Test
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10.1 Introduction
Consolidation is the process of time-dependent settlement of saturated clayey soil when
subjected to an increased loading. In this chapter, the procedure for one-dimensional laboratory
consolidation test will be described, and methods of calculation of obtaining the void ratio-pressure
curve (e vs. log p), pre consolidation pressure (p), and the coefficient of consolidation (Cv) will be
outlined.
10.4 Apparatus
Consolidation unit
Specimen trimming device
Wire saw
Balance, sensitive to 0.01 g
Stop watch
Moisture can
Oven.
58 | P a g e
5. Place the soil sample in the consolidation ring. Use the wire saw to trim the specimen flush with the
top and bottom of the consolidation ring. Record the size of the specimen.
6. Determine the weight of the consolidation ring and specimen (W2).
7. Saturate the lower porous stone on the base of the consolidometer.
8. Place the soil specimen in the ring over the lower porous stone.
9. Place the upper porous stone on the specimen in the ring.
10. Attach the top ring to the base of the consolidometer.
11. Add water to the consolidometer to submerge the soil and keep it saturated. In the case of the fixed
ring consolidometer, the outside ring (attached to the top of the base) and the stand pipe connection
attached to the base should be kept full with water. This needs to be done for the entire period of
the test.
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16. Repeat step 15 for soil pressure magnitude of 2 ton/ft2 (191.52 kN/m2), 4 ton/ft2 (383.04 kN/m2) and
8 ton/ft2 (766.08 kN/m2), etc. Note: In all cases p/p=1.
17. At the end of the test, remove the soil specimen and determine its moisture content.
10.6 Calculation
13. Collect all the time vs vertical dial readings data.
14. Determine the time for 90% primary consolidation, t90, from each set of time vs vertical dial readings.
15. Determine the time for 50% primary consolidation, t50, from each set of time vs vertical dial readings.
Determine the dial gauge reading corresponding to 50% primary consolidation as
+
=
2
16. Determine the height of solids of the specimen in the mold as
=
( )
Hs = height of solids
17. Determine the change in heights, H, of the specimen due to load increments from p to p + p
18. Determine the final specimen height, Ht(f), at the end of the consolidation due to a given loading.
19. Determine the height of voids, H, in the specimen at the end of consolidation due to a given loading,
p, as
20. = ( )
21. Determine the final void ratio at the end consolidation for each loading, p,
22. Determine the average specimen height, Ht(av), during consolidation for each incremental loading.
23. Calculate the coefficient of consolidation, Cv.
Where,
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H= maximum length of drainage path =
So,
0.848 × ( )
=
4
( ) =
% 0.197 = = ( )
[ ]2
0.197 ( )
=
4
25. Plot a semi logarithmic graph of pressure vs. final void ratio. Pressure p is plotted on the log scale,
and the final void ratio on the linear scale.
26. Calculate compression index, Cc. This is the slope of the linear portion of the e vs log p plot.
27. On the semi logarithmic graph, using the same horizontal scale, plot the values of cv.
28. Determine pre consolidation pressure, pc.
10.7 Result
The results of a consolidation test are often presented by plotting on the same sheet the log of pressure
against the following:
1. Void ratio, e
2. Coefficient of consolidation, cv,
3. Primary compression ratio, r.
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Height of soil solids. Hs = Weight of can + Dry specimen =
Loading
Unloading
Sample Calculation-
. .
Void ratio, ev= = .
= 0.505
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Bore Hole No.: 02 Sample No.: D-02
0.60
0.50
0.40
Void Ratio, e
0.30
0.20
0.10
0.00
1.00 10.00 100.00 500.00 1000.00 10000.00
Pressure, σ' (kPa)
Preconsolidation Pressure
= 500.0 kPa
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Bore Hole No.: 02 Sample No.: D-02 Sample Depth: 3.0 m
0.30
0.32
0.320
0.34
Deformation (mm)
0.36
0.364
0.38
0.40
0.407
0.42
0.44
0 1
1.30 10 22.50 100 1000 10000
Elapsed Time, t (min)
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Bore Hole No.: 02 Sample No.: D-02 Sample Depth: 3.0 m
0.20
0.25
Deformation (mm)
0.30
0.35
0.365
0.40
0.45
0 1.20 2 4 6 8 10
√(Elapsed Time, t) √(min)
. ( ) . × .
= = .
= 7.33
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Calculating compression index, Cc,
0.415 0.299
= = . = 0.200
.
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Triaxial Shear test
67 | P a g e
11.1 Introduction
Triaxial test is more reliable because we can measure both drained and untrained shear strength.
Generally, 1.4” diameter (3” tall) or 2.8” diameter (6” tall) specimen is used. Specimen is encased by a thin
rubber membrane and set into a plastic cylindrical chamber. Cell pressure is applied in the chamber (which
represents σ3’) by pressurizing the cell fluid (generally water).
Vertical stress is increased by loading the specimen (by raising the platen in strain controlled test and by
adding loads directly in stress controlled test, but strain controlled test is more common) until shear failure
occurs. Total vertical stress, which is σ1’ is equal to the sum of σ3’ and deviator stress (σd). Measurement of
σd, axial deformation, pore pressure, and sample volume change are recorded.
Depending on the nature of loading and drainage condition, triaxial tests are conducted in three different
ways.
i. UU Triaxial test
11.4 Apparatus
11.4.1 Special
30. A constant rate of strain compression machine of which the following is a brief description of one in
common use.
31. A loading frame in which the load is applied by yoke acting through an elastic dynamometer, more
commonly called a proving ring which used to measure the load. The frame is operated at a constant
rate by a geared screw jack. It is preferable for the machine to be motor driven, by a small electric
motor.
32. A hydraulic pressure apparatus including an air compressor and water reservoir in which air under
pressure acting on the water raises it to the required pressure, together with the necessary control
valves and pressure dials.
33. A triaxial cell to take 3.8 cm diameter and 7.6 cm long samples, in which the sample can be subjected
to an all-round hydrostatic pressure, together with a vertical compression load acting through a
piston. The vertical load from the piston acts on a pressure cap. The cell is usually designed with a
non-ferrous metal top and base connected by tension rods and with walls formed of Perspex.
68 | P a g e
11.4.2 General
i. 3.8 cm (1.5 inch) internal diameter 12.5 cm (5 inches) long sample tubes.
ii. Rubber ring.
iii. An open ended cylindrical section former, 3.8 cm inside diameter, fitted with a small rubber tube
in its side.
iv. Stop clock.
v. Moisture content test apparatus.
vi. A balance of 250 gm capacity and accurate to 0.01 gm.
Length:
Diameter:
69 | P a g e
Initial Area:
Initial Volume:
Cell pressure Strain dial Proving ring Load on Corrected area Deviator stress
reading sample
0.5 0
50
100
150
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