NHAI Bharatmala Pariyojna Report
NHAI Bharatmala Pariyojna Report
SUBMITTED BY SUBMITTED TO
Prashant Gautam Er. Jyoti Swaroop Pandey
2107190009007 Assistant Professor, AITM-CE
1
DECLARATRION
It is to declare that the internship report work published in this report entitled “NHAI
Bharatmala Pariyojna” is performed by Prashant Gautam under the guidance of
Er. Amit Chaursiya, Acchalganj, Unnao, Uttar Pradesh, the project work is original
and does not contain any material previously published or written by another
candidate. I further declare that to the best of my knowledge, the thesis does not
contain any part of the work which has been submitted for the award of any other
degree or diploma at Axis Institute of Technology and Management or any other
institution without due acknowledgment.
Prashant Gautam
2107190009007
2
ACKNOWLEDGEMENTS
I am extremely grateful and remain indebted to my guide Er. Amit Chaursiya for source of
inspiration and for his constant support in the formulation, implementation and evaluation of this
report. I am thankful to him for his constant constructive suggestions, which benefited me a lot in
developing this report. He had been a constant source of inspiration and motivation for hard work.
Through this column, it would be my utmost pleasure to express warm thanks to him for his
encouragement, cooperation and constant support without which I might have not been able to
accomplish this report.
I would also like to express my gratitude to PNC Inf. Ltd. for providing me the infrastructure to
carry out the Internship and to all staff-members who were directly or indirectly instrumented in
enabling me to stay committed for this project.
Prashant Gautam
2107190009007
3
CONTENTS
Certificate ........................................................................... 1
Declaration ......................................................................... 2
Acknowledgement ............................................................. 3
1. Introduction ........................................................................ 8
2. Safety Induction .................................................................. 9
3. Soil Tests .......................................................................... 11
Grain Size Analysis .................................................. 11
Liquid Limit .............................................................. 13
Plastic Limit and Plasticity Index ............................. 16
Modified Proctor Test ............................................... 18
Free Swell Index ....................................................... 21
4. Cement Test ...................................................................... 23
Consistency Test ....................................................... 23
Fineness Test ............................................................ 26
4
Initial & Final Setting Time ...................................... 27
5. Test on Bituminous Concrete ........................................... 29
GMM & Density of Asphalt Mixture........................ 29
Marshall Stability Test .............................................. 31
6. Learning Outcomes ........................................................... 34
5
LIST OF FIGURES
6
INDIAN STANDARD CODE USED:
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CHAPTER 1
INTRODUCTION:
National Highway Authority of India (NHAI) was constituted by an Act of Parliament in 1988
under the administrative control of the Ministry of Road Transport and Highways. NHAI has been
set up as a Central Authority to develop, maintain and manage the National Highways entrusted
to it by the Government of India.
PNC INFRATECH LIMITED is in the industry of Highway, Street, and Bridge Construction.
The project which is Lab Department “Rehabilitation and Up-gradation from 2 lanes to 4 lanes of
NH stretch under Bharatmala Pariyojna for Unnao-Lalganj section of New-31 (old NH-232A). I
have mainly done my internship training under the guidance of Quality engineer of PNC in the lab
department.
In Lab department, there are several important test has been done by the technician and quality
engineer. These lab work is much important because without testing, the amount of risk is more.
Firstly, there is some soil testing, these soil is use as the embankment and filling for the pavement.
In soil testing, check all the soil properties which can be affect to the pavement base.
After that, there is some aggregate testing for the right amount of aggregate which is suitable for
the pavement. Since the pavement is rigid pavement so there are several test for the cements which
is important for the good quality of cement which is use for the rigid pavement.
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CHAPTER 2
SAFETY INDUCTION:
On the jobsite, security is essential. The essential items for safety are a helmet, a jacket,
shoes, and gloves. These things improve the workers' health, safety, and working
conditions on the site. To avoid accidents and fatalities, safety procedures must be
implemented. Depending on whether you need to wear personal protective equipment or
not, the site is separated into a PPE zone and a non-PPE zone. There are various PPE and
safety items here.
HELMET
Helmet is the most important safety equipment. On the site it is compulsoryto all to wear
helmet, it protect our head which is very essential for us. There are some different types
of helmets are used on site.
Figure2.1
(Safety Helmets)
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SAFETY JACKET
The main function is to make the wearer visible in environments and circumstances where
there may be risks to their health and safety. Construction workers and those doing
maintenance on motorways, roads, or frequently wear reflective apparel.
Figure2.2
(Safety Jacket)
EYE PROTECTION
For the workers trained in welding (Face Shield), grinding, gas cutting, pouring concrete,
chipping, etc. work on a site, appropriate goggles must be ensured.
Figure 2.3
(Eye Protection)
SHOES
All participants in site operations are required to wear shoes with additional
traction soles and bonded seams.
Figure2.4
(Safety Shoes)
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CHAPTER 3
STANDARD
OBJECTIVE
APPARATUS
PROCEDURE
Sieve analysis of soil fraction passing 4.75 mm and retained on 75 microns IS sieve
Wet Analysis
Oven dry the portion of material passing 4.75 mm IS sieve at the temperature of 105 to
110°C.
Riffle the oven dried material so that a fraction of convenient mass of about 200 gm is
obtained.
Spread out the riffled and weighed fraction in a large tray or bucket and fill with water.
Add 2 gm of Sodium Hexametaphosphate gram of Sodium hydroxide and 1 gram of
Sodium carbonate per liter of water.
Thoroughly stir the sample and leave it for 24 hours soaking.
After the specified period of soaking, wash the sample thoroughly over 75 microns IS
sieves.
Continue washing until the water passing sieve is substantially clear.
Care shall be taken to see that the sieves are not over loaded in the process.
Oven dry at 105 to 110°C the sample and entry the fraction retained on each sieve which
is 4.75 mm, 2 mm, 425 microns, 75 microns.
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REPORT
PRECAUTION
Any particle may be tested to see if they will fall though but they shall not be pushed
though.
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3.1.2 LIQUID LIMIT:
STANDARD
OBJECTIVE
DEFINITION
Liquid Limit is defined as the water content at which the soil changes from liquid state to
plastic state.
APPARATUS
PROCEDURE
Take representative soil sample of approximately 120gms passing through 425 microns IS
sieve and mix thoroughly with distilled water in the evaporating dish to a uniform paste.
The paste shall have a consistency that will require 30 to 35 drops of the cup to cause the
required closure of the standard groove.
Leave the soil paste to stand for 24 hours to ensure uniform distribution of moisture
throughout the soil mass.
Remix the soil thoroughly before the test.
Place a portion of the paste in the cup above the spot where the cup rests on the base,
squeeze down and spread in to position with a few strokes of the spatula as possible and at
the same time trim to a depth of 1cm at the point of maximum thickness.
Make a clean, sharp groove by a grooving tool along the diameter through the centerline
of the cam follower.
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Drop the cup from a height of 10 + 0.25 mm by turning the crank at the rate of two-revolutions/
sec, until the two halves of the soil cake come in contact with the bottom of the groove along the
distance of about 12mm.
Record the number of drops required to cause the groove close for the length of 12mm.
Collect a representative slice of sample of soil approximately the width of spatula, extending from
about edge to edge of the soil cake at right angle to the groove in to an air tight container and keep
in the oven for 24hrs, maintained at a temperature of 1050 to 1100 C and express its moisture
content as the percentage of the oven dried weight.
Transfer the remaining soil in the cup to the evaporating dish and clean the cup and the grooving
tool thoroughly.
Repeat the operation specified above for at least three more additional trials (minimum of four in
all) with soil collected in evaporating dish to which sufficient water has been added to bring the
soil to more fluid condition.
Figure3.1
(Divided Soil Before Cut)
In each case record the number of blows and determine the moisture content as before.
The specimens shall be of such consistency that the number of drops required to close the
groove shall not be less than 15 or more than 35.
Figure3.2
(Soil Cake After Cut)
REPORT
Plot a flow curve with the points obtained from each determination on a semi logarithmic
graph representing water content on the arithmetical scale and the no of drops on the
logarithmic scale.
The flow curve is a straight line drawn as nearly as possible through the four or more
plotted points.
The moisture content corresponding to 25 drops as read from the curve shall be rounded
off to the nearest second decimal and is reported as liquid limit of the soil.
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PRECAUTIONS
This test should proceed from the drier (more drops) to the wetter (less drops) condition of
the soil.
This test may also be conducted from wetter to drier condition provided drying is achieved
by kneading the wet soil and not by adding dry soil.
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3.1.3 PLASTIC LIMIT AND PLASTICITY INDEX:
STANDARD
DEFINITION
Plastic limit is defined as minimum water content at which soil remains in plastic state.
APPARATUS
PROCEDURE
Take representative soil sample of approximately 20g from the portion of the material
passing 425 microns IS sieve and mix thoroughly with distilled water in an evaporating
dish till the soil mass becomes plastic enough to be easily molded with fingers.
In the case of clayey soils, leave the soil mass to stand for 24 hours to ensure uniform
distribution of moisture throughout the soil.
Form a ball with about 8 grams of this soil mass and roll between the fingers and the glass
plate as shown in Fig: 2.7.1 with just sufficient pressure to roll the mass into a thread of
uniform diameter throughout its length.
The rate of rolling shall be between 80 and 90 strokes/minute counting the stroke as one
complete motion of the hand forward and back to the starting position again.
Continue the rolling till the thread crumbles exactly at 3mm diameter.
If the soil thread doesn’t crumble exactly at 3mm knead the soil together to a uniform mass
and roll it again.
Continue this process of alternate rolling and kneading until the thread crumbles under the
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pressure exactly at 3mm diameter.
Collect the pieces of crumbled soil thread in an airtight container and determine its
moisture content.
Determine the plastic limit for at least two points of the soil passing 425 microns IS sieve.
REPORT
Report the individual and the mean of the results as the plastic limit of the soil to the nearest
second decimal.
PRECAUTIONS
At no time shall an attempt be made to produce failure at exactly 3mm diameter by allowing
the thread to reach 3mm then reducing the rate of rolling or pressure or both and continuing
the rolling without further deformation until the thread falls apart.
PLASTICITY INDEX
DEFINITION
The plasticity Index is defined as the numerical difference between its Liquid Limit and
Plastic Limit
REPORT
PRECAUTIONS
17
3.1.4 MODIFIED PROCTOR TEST:
STANDARD
IS-2720 (Part-8):1983 (Reaffirmed- May 2015)
OBJECTIVE
To obtain the graphical relationship of the “dry density’ to “moisture content” in the form
of “compaction curve”, for determining the values of Optimum Moisture Content (OMC)
and Maximum Dry Density (MDD).
DEFINITION
Optimum Moisture Content (OMC) is the water content at which the soil attains maximum
dry density.
Maximum Dry Density (MDD) is the dry density of soil corresponding to Optimum
Moisture Content.
APPARATUS
Proctor Mould (volume = 1000 cm3 for 100 mm diameter mould and volume= 2250 cm3
for 150 mm diameter mould (as per IS:10074-1982)
Metal rammer conforming to IS: 9189-1979. (weight = 4.9 kg)
Balance
Sieve 4.75mm, 19 mm and 37.5 mm I.S. Sieves
Oven
Steel Straight Edge
Airtight Container
PROCEDURE
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Weigh the mould with base plate attached, to the nearest 1g and record the weight as W1.
Attach the extension collar with the mould. Compact the moist soil into the mould in five
layers of approximately equal mass, each layer being given 25 blows, with the help of 4.9
kg rammer, dropped from a height of 450mm above the soil. The blows must be distributed
uniformly over the surface of each layer. The operator shall ensure that the tube of the
rammer is kept clear of soil so that the rammer always falls freely.
Figure3.3
(Modified Proctor Test)
After completion of the compaction operation, remove the extension collar and level
carefully the top of the mould by means of straightedge. Weigh the mould with the
compacted soil to the nearest 1 g and record this weight as W2.
Remove the compacted soil from the mould and place it on the mixing tray. Determine the
water content of a representative sample of the specimen. Record the moisture content as
‘M’.
The remainder of the soil shall be broken up and repeat Steps (iii) to (v) above, by adding
suitable increment of water to the soil. For sandy and gravelly soils, the increment is
generally 1% to 2% and for cohesive soils the increment is generally 2% to 4%. The total
number of determinations made shall be at least five, and the moisture contents should be
such that the optimum moisture content, at which the maximum dry density occurs, is
within that range.
For compacting soil containing coarse material up to 37.5 mm size, the 2250 cm3 mould
should be used. A sample weighing about 30 kg and passing the 37.5 mm IS sieve is used
for the test. Soil is compacted in five layers; each layer being given 55 blows of the 4.9 kg
rammer.
REPORT
The dry densities, γd, obtained in a series of determinations is plotted against the
corresponding moisture content ‘M’. A smooth curve is then drawn through the resulting
points and the position of the maximum on this curve is determined, which is called
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maximum dry density (M.D.D). And the corresponding moisture content is called optimum
moisture content (O.M.C.).
PRECAUTIONS
Soil should not contain excess moisture during the compaction process.
20
3.1.5 FREE SWELL INDEX:
STANDARD
IS 2720 (Part-40): 1977 (Reaffirmed 2021)
OBJECTIVE
Free swell is the increase in volume of a soil, without any external constraints, on
submergence in water.
APPARATUS
PROCEDURE
Take two representative oven dried soil samples each of 10 grams passing through 425-
micron sieve.
Pour each soil sample in to each of the two glass graduated cylinders of 100ml capacity.
Fill one cylinder with kerosene and the other with the distilled water up to the100ml
mark.
Figure3.4
(Free Swell Index)
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Remove the entrapped air in the cylinder by gentle shaking and stirring with a glass
rod.
Allow the samples to settle in both the cylinders.
Sufficient time, not less than 24 hours shall be allowed for soil sample to attain
equilibrium state of volume without any further change in the volume of the soils.
Record the final volume of the soils in each of the cylinders.
REPORT
Read the level of the soil in the kerosene graduated cylinder as the original volume of the
soil samples, kerosene being non polar liquid does not cause swelling of the soil.
Read the level of the soil in the distilled water cylinders as free swell level.
Record the individual and the mean results to the nearest second decimal.
PRECAUTION
In the case of highly expansive soils such as Sodium Betonites. the sample size may be 5
grams or alternatively a cylinder of 250ml capacity for 10 grams of sample may be used.
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CHAPTER 4
The standard consistency of a cement paste is defined as that consistency which will permit
the vicat plunger to penetrate to a point 5 to 7mm from the bottom of the vicat mould.
APPARATUS
PROCEDURE
Unless otherwise specified this test shall be conducted at a temperature 27 + 20 C and the
relative humidity of laboratory should be 65 + 5%.
Prepare a paste of weighed quantity of cement (300gms) with weighed quantity of potable
or distilled water, taking care that the time of gauging is not less than 3minutes nor more
than 5minutes and the gauging is completed before any sign of setting occurs.
The gauging is counted from the time of adding water to the dry cement until commencing
to fill the mould.
Fill the vicat mould with this paste resting upon a non-porous plate.
Smoothen the surface of the paste, making it level with the top of the mould.
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Slightly shake the mould to expel the air.
In filling the mould operators’ hands and the blade of the gauging trowel shall only be used.
Immediately place the test block with the non-porous resting plate, under the rod bearing
the plunger.
Lower the plunger gently to touch the surface of the test block and quickly release, allowing
it sink into the paste.
Prepare trial pastes with varying percentages of water and test as described above until the
plunger is 5mm to 7mm from the bottom of the vicat mould.
Figure4.1
(Consistency Test)
REPORT
Express the amount of water as a percentage by mass of dry cement to the first place of
decimal.
24
PRECAUTION
Care shall be taken to maintain the specified temperature, humidity and the time of mixing
so as to avoid setting of cement paste.
25
4.1.2 FINENESS TEST:
STANDARD
IS: 4031 (Part 3) 1988
OBJECTIVE
26
4.1.3 INITIAL & FINAL SETTING TIME:
STANDARD
IS: 4031 (Part 5) 1988
OBJECTIVE
27
Final Setting Time
• Replace the needle of the vicat apparatus by the needle with an annular ring Lower the
needle and quickly release.
• Repeat the process until the annular ring makes an impression on the mould.
• Record the period elapsed between the time of adding water to the cement to the time when
the annular ring fails to make the impression on the mould as the final setting time.
REPORT
• Report the initial setting time and final setting time in minutes.
PRECAUTIONS
• The time of gauging in any case shall not be less than 3 minutes not more than 5 minutes.
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CHAPTER 5
STANDARD
AASHTO T 209
OBJECTIVE
To determine the specific gravity and density of asphalt mixture (bituminous & aggregate)
APPARATUS
Balance or scale: 10,000 g capacity, readable to 0.1 g, meeting AASHTO M 231, Class G2
Container: A glass, metal, or plastic bowl, pycnometer or volumetric flask between 2000
and 10,000 mL as required by the minimum sample size requirements in Table 1 sample
and capable of withstanding full vacuum applied
Pycnometer / volumetric flask covers: A glass plate or a metal or plastic cover with a vented
opening
Vacuum lid: A transparent lid with a suitable vacuum connection, with a vacuum opening
to be covered with a fine wire mesh
Vacuum pump or water aspirator: Capable of evacuating air from the container to a residual
pressure of 3.4 kPa (25 mm Hg)
Vacuum measurement device: Residual pressure manometer or vacuum gauge, capable of
measuring residual pressure down to 3.4 kPa (25 mm Hg) or less and accurate to 0.1 kPa
(1 mm Hg)
Manometer or vacuum gauge: Capable of measuring the vacuum being applied at the
source of the vacuum
Water bath: A constant-temperature water bath (optional for Pycnometer or Volumetric
Flask Method)
Thermometers: Thermometric devices accurate to 0.25°C (0.5°F) and with a temperature
range of at least 20 to 45°C (68 to 113°F).
Bleeder valve to adjust vacuum
Automatic vacuum control unit (optional).
Timer
Towel
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PROCEDURE
Separate the particles of the sample, taking care not to fracture the mineral particles, so that
the particles of the fine aggregate portion are not larger than 6.3 mm (1/4 in.). If the mixture
is not sufficiently soft to be separated manually, place it in a large flat pan and warm in an
oven only until it is pliable enough for separation.
Cool the sample to room temperature.
Determine and record the mass of the dry container to the nearest 0.1 g.
Place the sample in the container.
Determine and record the mass of the dry container and sample to the nearest 0.1 g.
Determine and record the mass of the sample by subtracting the mass determined in Step
3 from the mass determined in Step 5. Designate this mass as “A.”
Add sufficient water at approximately 25 C (77 F) to cover the sample by about 25 mm (1
in.).
Figure5.1
(Density Test)
Place the lid on the container and attach the vacuum line. To ensure a proper seal between
the container and the lid, wet the O-ring or use a petroleum gel.
Remove entrapped air by subjecting the sample to a partial vacuum of 3.7 ±0.3 kPa (27.5
±2.5 mm Hg) residual pressure for 15 ±1 minutes.
Agitate the container and sample, either continuously by mechanical device or manually
by vigorous shaking at 2-minute intervals. This agitation facilitates the removal of air.
Release the vacuum. Increase the pressure to atmospheric pressure in 10 to 15 seconds if
the vacuum release is not automated. Turn off the vacuum pump and remove the lid. When
performing the pycnometer / volumetric flask method, complete steps 12B through 16B
within 10 ±1 minute.
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5.1.2 MARSHALL STABILITY TEST:
STANDARD
AASHTO T 209
OBJECTIVE
To determine the stability, flow, voids, voids in mineral aggregates, voids filled with
asphalt and density of the asphalt mixture by Marshall stability test.
APPARATUS
31
The material is compacted with 50 blows of the hammer (or as specified),
and the sample is inverted and compacted in the the other face with same
number of blows.
After compaction, the mould is inverted. With collar on the bottom, the base
is removed and the sample is extracted by pushing it out the extractor.
The sample is allowed to stand for the few hours to cool.
The mass of the sample in air and when submerged is used to measure the
density of specimen, so as to allow, calculation of the void properties.
PROCEDURE
Specimens are heated to 60 ±1oC either in a water bath for 30-40 minutes or in an oven for
minimum of 2 hours.
The specimens are removed from the water bath or oven and place in lower segment of the
breaking head. The upper segment of the breaking head of the specimen is placed in
position and the complete assembly is placed in position on the testing machine.
The flow meter is placed over one of the post and is adjusted to read zero.
Figure5.2
(Marshall Stability Test)
32
Load is applied at a rate of 50 mm per minute until the maximum load reading is obtained.
The maximum load reading in Newton is observed. At the same instant the flow as recorded
on the flow meter in units of mm was also noted. Specimens are heated to 60 ±1oC either
in a water bath for 30-40 minutes or in an oven for minimum of 2 hours.
The specimens are removed from the water bath or oven and place in lower segment of the
breaking head. The upper segment of the breaking head of the specimen is placed in
position and the complete assembly is placed in position on the testing machine.
The flow meter is placed over one of the post and is adjusted to read zero.
Load is applied at a rate of 50 mm per minute until the maximum load reading is obtained.
The maximum load reading in Newton is observed. At the same instant the flow as recorded
on the flow meter in units of mm was also noted.
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LEARNING OUTCOMES
34