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1 UNESCO-NIGERIA TECHNICAL & VOCATIONAL EDUCATION REVITALISATION PROJECT-PHASE II YEAR 2- SE MESTER 2 PRATICAL/ Version 1: December 2008 NATIONAL DIPLOMA IN CIVIL ENGINEERING TECHNOLOGY INTRODUCTION TO HIGHWAY ENGINEERING COURSE CODE: CEC 204

Cec 204 Practical

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Page 1: Cec 204 Practical

1

UNESCO-NIGERIA TECHNICAL &

VOCATIONAL EDUCATION

REVITALISATION PROJECT-PHASE II

YEAR 2- SE MESTER 2

PRATICAL/

Version 1: December 2008

NATIONAL DIPLOMA IN

CIVIL ENGINEERING TECHNOLOGY

INTRODUCTION TO HIGHWAY

ENGINEERING

COURSE CODE: CEC 204

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Table of Contents

WEEK 1 Standard Flakiness and Elongation Test

WEEK 2 Aggregate Crushing Value (ACV) Test

WEEK 3 Aggregate Impact Value (AIV) Test

WEEK 4 Hardness Test

WEEK 5 Viscosity Test

WEEK 6 Flash and Fire Points Test

WEEK 7 Ductility Test

WEEK 8 Softening Point (Ring and Ball Test)

WEEK 9 Stability and Flow Test (Marshall)

WEEK 10 Hubbard Field Test

WEEK 11 Design Mix of Plastic Concrete

WEEK 12 Design of Trial Mix of Plastic Concrete

WEEK 13 Stability Test (Hveem Stabilometer)

WEEK 14-15 Site Visit

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INTRODUCTION TO HIGHWAY ENGINEERING PRATICAL

INTRODUCTION

The properties of most importance in a road making aggregate are its resistance to crushing,

impact, abrasion and polishing, it s specific gravity and water absorption and its grading and

particle shape.

As aggregate obtained from different sources differ considerably in their constitution and

properties, inevitably they differ also with their engineering properties. It is necessary

therefore, to carry out various tests on aggregates to ensure not only that undesirable

materials are excluded from highway pavements but also that the best available aggregates

are included.

Also for bitumen and tars, the most careful specifications with regard to the design and

construction of a bituminous road surfacing are of little value if the properties of the

bituminous binder used in the design are not adequately controlled. To ensure that the

material obtained has the desired qualities, a number of tests have been devised which

attempts to measure various binder properties for particular reasons.

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WEEK I AGGREGATES (BS 812)

EXPERIMENT NO.1: STANDARD FLAKINESS AND ELONGATION TESTS

AIM: To determine the Flakiness and Elongation indices of a sample

of aggregate.

APPARATUS: 1. A thickness gauge and a length gauge

2. A 3kg balance

3. One set of sieves of sizes: 63.5mm, 50. 8mm, 38.1mm,

254mm, 19.05mm, 12.7mm, 9.52mm and 6.35mm

4. A shallow tray.

THEORY: A flaky particle has thickness (least dimension) less than 0.6

times the mean size of the fraction to which the particle

belongs. An elongated particle has length which is more than

1.8 times the mean sieve size of the sieve fraction to which the

particle belongs. The content of elongated or flaky particles in

excess of 10 to 15 percent of the weight of coarse aggregate is

generally considered undesirable.

PROCEDURE: 1. Sieve a sufficient but known quantity of coarse aggregate to

Provide a minimum of 200 pieces on each of the above sieves.

2. Separate the flaky material of each fraction by “placing” on the

thickness gauge and determine the total weight in the

appropriate slot of material.

3. Weigh the total amount of material passing the gauge to an

accuracy of at least 0.1% of the weight of the test sample.

4. Repeat, using the length gauge.

RESULTS: Report the flakiness index as the total weight of material

passing the various thickness gauges expressed as a percentage

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of the total weigh of the sample gauge to the nearest whole

number. Obtained also the elongation Index.

CONCLUSION: Comment on your results and state their compliance or

otherwise with standard values.

REFERENCE: BS 882

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WEEK 2

AGGREGATES (BS 812: Part 3)

EXPERIMENT NO.2: DETERMINATION OF AGGREGATE CRUSHING

VALUE (ACV)

AIM: To determine the aggregated crushing value of a sample of

coarse aggregate.

APPARATUS: 1. A 152mm dia open- ended steel cylinder with plunger and

base plate.

2. A tamping rod of 9.5mm dia and 609.6mm long.

3. A 3kg balance

4. A set of B.S test sieves of sizes: 12.7mm, 9.5mm and 2.0mm.

PROCEDURE: 1. Sieve the aggregate sample to pass through sieve size

21.7mm and retained on the B.S sieve 9.5mm.

2. Prepare sufficient aggregate for tests (about 5 kg) and ensure

that it is in a clean and surface dry condition (according to

standard requirement, it should be oven –dried, 100 – 110oC).

3. Place the cylinder on the base plate and fill with the aggregate

in three equal layers giving 25 blows to each layer.

4. Level off the top of the aggregate with the tamping rod and

weigh (weigh A). Insert the plunger so that it just rests

horizontally on the surface of the aggregate.

5. Test sample in the compression machine loading at 40 KN/min

to a load of 400 KN (10 minutes).

6. Remove the material from the cylinder and sieve of a 2.40mm

B.S test sieve.

7. Determine the weight of the fines passing the 2 sieve (weight

B) and express this as a percentage the total weight of

aggregate used as shown in the calculation below.

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CALCULATIONS: Aggregate crushing value = B x 100

A

RESULTS: Report the mean of the two values to the nearest number.

Permissible crushing value is as for impact test.

CONCLUSION: Comment on your results and compare with the permissible

values.

REFERENCE: BS 882

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WEEK 3 AGGREGATES (BS 812: Part 3)

EXPERIMENT NO.3: DETERMINATION OF AGGREGATE IMPACT VALUE

AIM: To determine the impact of a sample of coarse aggregate.

APPARATUS: 1. An aggregate impact testing machine complete with standard

cylindrical measure of 76.2mm dia and 50.8mm high and

tamping rod of 9.5mm dia and 228.6mm long.

2. A set of B.S test sieves: 12.7mm, 9.52mm and 2.40mm.

3. A 3kg balance

THEORY: The impact value is expressed as percentage of fines passing

the 2.40mm sieve (to the nearest who le number) to total weight

of the sample. The permissible AIV is 45% for ordinary

concrete used for wearing surfaces

.

PROCEDURE: 1. Prepare a sample of the coarse aggregate which passes

The 12.7mm sieve and is retained on the 9.52mm sieve.

2. Prepare sufficient aggregate for two tests and ensure that it is in

a clean and surface dry condition.

3. Fill the 76.2mm dia cylinder in three equal layers giving 25

strokes of the 22.9cm metal tamping rod to each layer.

4. Level off the top of the aggregate to the nearest gram and use

the same weight of material for each test (weight A).

5. Place the whole of the sample in the cup, fix firmly in position

on the base on the impact machine, and apply 25 blows of the

tamping rod.

6. Subject the sample to 15 blows by allowing the hammer of the

machine to fall freely.

7. Sieve the crushed aggregate on a 2.40mm sieve and determine

the percentage passing by weight (weight B).

CALCULATIONS: Aggregate impact value = B x 100

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A

RESULTS: Report the mean of the two tests.

CONCLUSION: Comment on your results by comparing them with the standard

values.

REFERENCE: BS 882

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WEEK 4

EXPERIMENT NO.4 HARDNESS TEST (ABRASION TEST)

AIM: To determine the hardness of a sample of aggregate.

APPARATUS: Los Angeles Abrasion machine weighing balance, 1.7mm

sieve.

THEORY: The top layers of a pavement get abraded due to the movement

of tires. A material which is highly abrasion resistance has a

long life. The test has been standardized as ASTM-C 131 and

AASHTO –T 96.

PROCEDURE: 1. Weigh 5kg dried of test sample.

2. Place the weighed sample into the steel cylinder along with the

required steel balls.

3. Rotate the cylinder at a speed of 30 -33 revolutions/minute for

500 – 1000 revolutions (depending on the material).

4. Remove the material

5. Pour into 1.7mm sieve

6. Weigh the material that passes through 1.7mm

RESULT: Report the weight of this material (fines) as a percentage of the

total weight of the sample. This is known as Los Angeles

Abrasion value.

CONCLUSION: Comment on your results and state their compliance or otherwise with

standard values.

WK 5

EXPERIMENT NO.5: VISCOSITY TEST

THEORY: Viscosity of a liquid is the property that retards flow; so that

when a force is applied to a liquid, the higher the viscosity, the

slower will be the movement of the liquid. Viscosity of

bituminous binder is its most important characteristic. Hence,

viscosity measurements are useful not only in ensuring that

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material with the desired consistency has been obtained but

also as a means of selecting binders for specific use.

APPARATUS: 1. Saybolt Furol Viscometer

2. Bath equipped with stirring and heating receiver

3. Oil tube thermometer

4. Timing device

5. Withdrawal tube or pipette

SAMPLE PREPARATION: Filter the material through a 100 mesh (150 micron) wire

strainer.

PROCEDURE: 1. Pour into container the quantity of material to be tested and

allow it to be draw.

2. Insert the cork stopper and pour material into the cup.

3. When the temperature of the bath and cup are steady or remain

constant, withdraw the thermometer and insert the tip of the

withdrawal tube at the point in the gallery.

4. Place the receiving flask in position. Snap the cork from its

position and at the same time start the timer.

5. Stop the timer when the bottom of the meniscus of the liquid

reaches the mark on the neck of the graduating receiving flask.

6. Record in seconds the time it takes for the 60ml of the oil to

flow by gravity from the completely filled cylinder as the

viscosity.

REFERENCE: AASHTO 72 – 68.

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WEEK 6

EXPERIMENT NO.6: FLASH AND FIRE POINTS (CLEVEALAND OPEN UP)

THEORY: The flash and fire point test are indirect reflections of binder

volatility. The flash point is the more important of two, because

it indicates the maximum temperature to which the binder can

be safely heated.

APPARATUS: Cleveland open cup, Bunsen burner.

PROCEDURE: 1. Fill the cup with the material to be tested.

2. Light and adjust the test flame.

3. Place and test flame under the cup with the material to be

tested, thus the material is heated in the open cup.

4. At intervals a small flame is applied near its surface. The time

consumed in passing the flame across the cup shall be about 1

second.

5. Record as the flashpoint the temperature read on the

thermometer at which the material gives so much vapour that

will get temporarily or momentary ignite or flash on

application of a small pilot flame.

6. To determine the fire point, continue heating so that the sample

temperature increases at a rate of not less than 5oC or more than

6oC per minute.

7. Continue application of pilot flame until the vapour continues

to burn for a period of at least 5 seconds.

8. Record the temperature at which this occurs as the fire point.

REFERENCES: ASTM Standard 1958 part 4 D92

AASHTO T.48.

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WEEK 7

EXPERIMENT NO.7: DUCTILITY TEST

THEORY: The ductility test is a measure of the internal cohesion of

bitumen. Bitumen possessing high ductility is normally

cementitious and adheres well to aggregate. The test is used as

a measure of the flexibility of the binder under slowly applied

load.

APPARATUS: Briquette brass mould, water bath, testing machine

PROCEDURE: 1. completely melt the bituminous material by heating it in an oil

bath maintained at minimum temperature needed to properly

liquefy the sample (for paving asphalt cements, the oil bath

shall be maintained at a temperature of 150 – 180oC.

2. Strain the melted sample through a No.50 (297 micron) sieve.

Stir thoroughly and pour into the mould. Assembly the mould

on a brass plate, and to prevent the material under test from

sticking, thorough amalgamate the surface of the plate and

interior surface of the sides of the mould.

3. Let the mould containing the material cool to room

temperature. Place it in the water bath maintained a temperature

of 25+0.5oC.

4. By means of a warm knife or spatula cut off the excess bitumen

to make the material just level full in the mould.

5. After the mould with briquette specimen had been in the water

for 1 ½ hours, remove the briquette from the plate, detach the

side pieces.

6. Transfer to the testing machine. Attach the rings at each side of

clips or pins to the hook in the testing machine and pull the two

clips apart at a uniform speed of 5cm/min.

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7. Measure the distance in cm through which the clips have been

pulled to produce rupture. The test is carried out under water,

maintained at the test temperature in the ductilometer.

8. The average of three normal tests is the ductility of the sample.

9. Adjust the specific gravity of the bath (if necessary) by the

addition of sodium chloride so that the bituminous material

neither comes to the surface of the water, nor touches the

bottom of the bath at any time during the test.

REFERENCE: ASTM Standards 1958 part 4 D 113

Test Methods

ASTM 113, ASSHO T 51 –, J.P 32

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WEEK 8

EXPERIMENT NO.8: SOFTENING POINT (RING AND BALL TEST)

THEORY: The specifications of many bituminous blinders for particular

purposes are often written without softening point requirement.

It is used to specify hard bitumens and it helps to characterize

its rate of setting. It may indicate the tendency to flow in

service in the case of thick films.

APPARATUS: A brass ring, a 9.5mm steel ball, ball guides, a glass beaker,

rings support, thermometer and stirrer

SAMPLE PREPARATION:

1. Heat the bitumen in a suitable vessel to 75 – 100oC above the

expected softening point and stir.

2. Heat the rings to approximately the same temperature.

3. Place them on a smooth metal plate covered with a coating of

glycerol and dextrin mixture to prevent the bituminous

material adhering to it overfill each ring with bitumen.

4. Allow to cool for 3mins, cut off the excess of bitumen with a

warmed knife, leaving it level.

5. Proceed with test within 4 hrs.

PROCEDURE: Materials having softening points 80oC or below

(a) Assembly of Apparatus: Fill in the glass beaker to a depth of 100mm with freshly boiled

distilled water (boiled to expel air). The water should be cooled

to 5oC.

1. Suspend the ring containing the sample in the water so that the

lower surface of the filled ring is 25mm above the upper

surface of the lower horizontal plate which is 12.5mm above

the bottom of the glass beaker.

2. Maintain the initial temperature of water for 15mins.

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3. With forceps, place the ball in the centre of the upper surface of

the bitumen in the ring.

(b) Heating: Heat the water gently at about 5oC/mm, string. Avoid the

effects of draughts using shield if necessary. The rate of rise in

temperature shall be uniform; and shall not be average over the

period of the test. The maximum permissible variation in

temperature after the first three should not be average over the

period of the test. The maximum permissible variation in

temperature after the first three should not be more than 1oC.

Reject all tests in which the rate of rise exceeds these limits.

(c) Softening Point: Record as the softening point the temperature of the

thermometer at the instant the bituminous material touches the

horizontal plate.

Materials having softening points above 80oC: Use the same

procedure as described above except fill the bath with glycerin.

The starting temperature of the glycerin bath shall be 32oC.

Typical result 55oC, 56

oC, average 56½

oC, such bitumen would

be suitable for rolled asphalt, 50 – 75oC is required (BS 1418)

for DPC and tanking in mastic asphalt; 60 – 110oC are limit

for flooring (BS 1410), again mastic asphalt.

REFERENCES: ASTM Standard 1958, part 4, D-36

Bituminous materials in road construction

Road research laboratory.

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WEEK 9

EXPERIMENT NO.9: STABILITY AND FLOW TEST

PRACTICAL SIGNIFICANE: Bitumen is extensively used for road construction, to

therefore aid in ensuring that bitumen has the desired quality

and that the optimum qualities of materials are used, optimum

bitumen content has therefore become a very important study

for determining the stability and resistance to plastic flow of the

bitumen.

APPARATUS: Marshall Apparatus which consists of the following part

1. Specimen and mould assembly with base plate and extension

collar

2. Specimen extractor

3. Compaction hammer

4. Specimen mould holder

5. Breaking head assembly

6. Loading jack

7. Compaction pedestal

8. One proving ring of 2700kg capacity complete with mounting

block and dial micrometer.

SAMPLE PREPARATION

1. Dry aggregates to constant weight at 105 to 110oC and separate

the aggregates by dry sieving into desired fraction.

2. Weight into separate pans, for each test specimen the amount of

each fraction required to produce a batch that will result in the

compacted specimen of 6.35cm in height and 10.16cm in

diameter.

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3. Place the pan in hot plate and heat to a temperature of about

27oC above the mixing temperature.

4. Charge the mixing bowl with the heated aggregates and weigh

the required amount of bituminous material within the limit of

the mixing temperature. Mix the aggregate and bituminous

material rapidly until thoroughly coated.

PROCEDURE: 1. Clean the specimen mould assembly and the face of the

Compaction hammer and head immersed them either in boiling

water or on the hot plate to a temperature between 100oC and

150oC.

2. Place a piece of filter paper cut to the size in the bottom of the

mould before the mixture is introduced.

3. Place the entire batch into the mould; stir the mixture

vigorously with a heated spatula.

4. Replace the collar, and place the mould assembly on the

compaction pedestal and apply 50 blows with the compaction

hammers with the free fall of 45cm for a tyre pressure of

0.7MN/m2 and 75 blows for a tyre pressure of 1.4MN/m

2.

5. Remove the base plate and place the sample extractor on the

end of the specimen.

6. Place the assembly with the extension collar up to the testing

machine.

7. Apply pressure to the collar by means of the load transfer bar

and force the specimen into the extension collar and lift the

collar from the specimen.

8. Carefully transfer to a smooth, flat surface and allow it to stand

overnight at room temperature.

9. Weigh, measure and test the specimen.

10. Bring the specimens to the desired temperature by immersing

them in the water bath for 30 to 40 minutes. (The specified

temperature is 60oC for asphalt specimen and 38

oC for tar

specimen.

11. Remove the specimen from the water bath, dry and carefully

place it in lower testing head.

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12. Place the upper head on the specimen. Then place the complete

assembly in position on the testing machine.

13. Place the dial micrometer in position over one of the guide rods

and adjust the flow meter reading to zero.

14. Hold the meter sleeve firmly against the upper segment of the

breaking head while the test load is being applied.

15. Apply the load on the specimen by means of a constant rate of

movement of the load jack or testing machine head at 5cm per

minute until the maximum is reached and the load decreases as

indicated by the dial.

16. Note and record the indicated flow value in terms of 0.25mm if

a micrometer dial is used to measure the flow.

17. The elapsed time for the test from the removal of the test

specimen from water bath to the maximum load determination

should not exceed 30 seconds.

18. The maximum load is the measure of stability.

RESULT: Report as findings

The report should include the following information for each

specimen test,

1. Height of the test specimen

2. Maximum load at failure

3. Flow value in multiple of 0.25m

4. Mixing temperature

5. compacting temperature

6. Test temperature

7.

TEST METHOD : ASTM D 1559 – 60

REFERENCES: 1. British Standard 3235 1984 – Test methods for bitumen

2. ASTM standard

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WEEK 10

EXPERIMENT NO.7: HUBBARD FIELD TEST

AIM: To test the resistance to plastic flow of compressed bituminous

mixture.

APPARATUS: 1. Cylindrical moulds 5cm in diameter for preparing the

Specimen 5cm

2. Two plungers, one for the top end one for the bottom per

mould.

3. Pan and knife for heating and mixing bitumen and aggregate

4. Weighing balance

5. Compacting and loading unit of capacity 500kg and travel of

tension rod at a uniform rate of 6cm per minute.

PROCEDURE: 1. Take 90gm of sand, 10gm of cement and 5gm of bitumen.

2. Heat sand and cement on a container and add 5gm of hot

bitumen.

3. Mix thoroughly.

4. Place the bottom plunger into the mould. Put the mix on the

mould so that the height of the specimen is 2.5cm+0.125cm.

5. Put the top plunger over the mix and place in position in the

compacting machine and apply a load of 225kg. (This is

indicated by 75 divisions of the strain gauge).

6. Take out the mould and place it in cold water for one hour and

take out the sample.

TESTING OF SPECIMEN

1. Place the specimen in the test mould assembly over the test ring

with plunger on the top.

8. Apply the compressive load at a constant rate of deformation of

6.0cm per minute.

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RESULT: Report the failure value of the strain and determine the

failure load.

CONCLUSION: Comment on your result and state their compliance or

otherwise with stander value.

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WEEK 11

EXPERIMENT NO.11: DESIGN TRIAL MIX OF PLASTIC CONCRETE

THEORY: The most popular method of mix design is eh Marshall method.

The Hveem stabilometer is less used. Other methods are the

Hubbard field and Smith triavial.

Marshall method uses standard test specimens of 6.35cm

height and 10.16cm diameter. The principal features of the

method are a density-void analysis and stability flow test of the

compacted specimen.

PROCEDURE: The test specimens are prepared with varying asphaltic cement

content with ½% increments such that at least two values are

above and two below the optimum. Usually 6 values of

asphaltic cement content are selected and for each three

specimens are needed. The specimens are prepared by heating

the aggregates and buder and mixing them both top and bottom

by the hammer. The procedure is adequate for highway

pavements designed for a type pressure of 0.7MN/m2. For

airfield pavements and heavily trafficked highway pavements

designed for a tyre pressure of 1.4MN/m2, 75 blows are given

on each face. The Marshall testing machine is an electrically

powered testing device design to apply loads at a constant rate

of strain of 5cm per minute and equipped with a calibrated

proving ring to measure the load. The machine measures both

stability and flow that developed at failure. The measured

stability values are next corrected to those which would have

been obtained if the specimen has been exactly 63.5mm high.

This is done by multiply correlation value.

DENSITY VOID ANALYSIS: The theoretical specific gravity (density) GM for void less

bituminous paving mixtures is determined by

GM = 100

W1 + W2 + W3 ……….Wn

G1 G2 G3 Gn

Where

W1 = the percentage by weight of bitumen

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G1 = the specific gravity of bitumen

W2, W3 =…Wn = percentages by weight of different aggregate

fractions.

G2………. Gn = specific gravities of the respective aggregate

fraction.

The procedure for determining d, the bulk specific gravity of a

compacted specimen is given in AASHTO T – 166 as

d = A

B – C

Where

A = weight of the dry specimen in air in grams

B = weight of saturated surface dry specimen in air, in grams.

C = weight of saturated specimen in water, in grams.

If the specimen has an open and porous surface, it must be

covered with a paraffin coating before being in the water. The

formula for determining d, the bulk specific gravity of a

compacted asphaltic mixture when the specimen is coated with

paraffin is as thus follows:

d = A

D – E – D – A

F

Where

A = weight of the dry specimen in air, in grams

D = weight of the specimen plus paraffin coating in air, in

grams.

E = weight of the specimen plus paraffin coating in water, in

grams.

F = bulk specific gravity of the paraffin

The percentage of voids (V.T.M) in an actual paving mixture is

determined by

V.T.M = (Gm – d) x 100

Gm

V.T.M = voids in the total mixture is d in the specimen %.

Again, for each specimen, calculate the percentage of voids in

the compacted mineral aggregate frame work which is filled

with the binder. This involves first determining the amount of

Page 24: Cec 204 Practical

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voids in the aggregate framework (V.M.A) and then calculating

the percentage filled with binder material.

The V.M.A is obtained by subtracting the volume occupied by

the aggregate in the compacted specimen from the bulk volume

of the compacted specimen, i.e. the volume of voids which in

theory is available for filling with binder. Thus,

V.M.A = V - VE – VF VMF

Where W - Wc - Wf - Wmf

D Gc Gf Gmf

V.M.A = voids in the mineral aggregate framework cm3

V = volume of specimen, cm3

Vc = Vf Vmf = volume of coarse, fine and mineral filler

fraction, respectively, of the aggregates in the specimen, cm3.

W = weight of the specimen, gm

Wc, Wf and Wmf = weight of coarse, fine and mineral filler

fractions respectively of the aggregates in the specimen, gm.

Gc, Gf and Gmf = Apparent specific gravities of coarse, fine and

mineral fractions respectively, of the aggregate in the specimen.

The voids in the mineral aggregate framework are often

expressed as a percentage of the total volume of the specimen.

Thus

% V.M.A = V.M.A x 100

V

In order to obtain individual binder content for stability, flow,

density and voids, separate graphical plots are prepared for the

following;

(a) Binder content versus marshall stability

(b) Binder content versus marshal flow

(c) Binder content versus percentage of voids in the total

mix

(d) Binder content versus percentage of voids in the mineral

aggregate framework filled with binder.

(e) Binder content versus unit weight

For illustrate purposes the data in Table 11.1 are plotted in fig

11.1 and t eh points joined with smooth curves.

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25

Table 11.1 Typical Marshall Test Data

Binder content

% Stability KN Flow Units Percentage of air

voids in the total

mixture

Percentage of

filled voids in

the aggregate

framework

Unit weight

kg/m3

3 4.89 8.9 12.5 34 2169

4 7.06 9.4 7.2 65 2207

5 8.06 11.8 3.9 84 2255

6 7.52 14.6 2.4 91 2227

7 6.49 19.2 1.9 93 2190

8000

7000

6000

5000

2 4 6 8

.

. .

.

Sta

bili

ty N

5

2 4 6 8

4

3

2

1

0

. .

. . .

Mars

hall

flow

m

m

20

10

0

2 4 5 7

. .

.

.

Void

s in

tota

l m

ix %

100

50

20

2 5 8

.

.

.

.

Aggre

gate

void

s file

d

with bin

der

%

2300

2250

2200

2 5 7

Unit w

t kg/m

3

. . .

.

Page 26: Cec 204 Practical

26

The next stage involves the determination of optimum binder

content. From these curves, the individual binder content is

determine d for the following conditions

(a) max stability

(b) max unit wt

(c) median limit or percent air void

The numerical average binder content from these three is taken

as the optimum binder contended is used in design, provided it

gives a mixture that satisfies the established criteria. The

marshall criteria normally adopted for design are given in Table

11.2.

For the illustrative data, the optimum binder content is found

as:

Property Unit weight Stability V.T.M

Binder content % 5.0 5.0 4.9

The optimum binder content is taken as the average of these

three binder.

i.e. 5 + 5 + 49 = 4.97

3

4.97% is the optimum binder content for the mix.

Table 11.2 Design criteria for Marshall method of design.

Traffic category Heavy (Tyre pressure

1.4MN/m2)

Medium (Tyre pressure

0.75MN/m2)

Pavement use Airport pavement and

heavily trafficked

highways

Highways with low

traffic

No of blows at each

end of specimen 75 50

Stability 650 200 Flow 10.25mm 16max 20max % air voids 3 – 5 3 – 5 % voids in

aggregate filed with

bitumen

75 – 82 72 – 85

Page 27: Cec 204 Practical

27

WEEK 12

EXPERIMENT NO.12: DESIGN OF TRIAL MIX OF PLASTIC CONCRETE

CLASS ACTIVITY: A specimen of asphaltic concrete has a height of 6.20cm and a

diameter of 10.16cm, the weight of the compacted specimen

(uncoated) in air is 1174.4gms and in water, the weight is

668.4gms. When coated with paraffin, its weight in air is

1220.9gms and its weight when immersed in water is

664.4gms. The specific gravity of paraffin is 0.90. The analysis

of the specimen yielded the following:

S/No Material Specific

gravity

Mix composition

(% by weight of

total mix)

Aggregate

composition (%

by weight of total

aggregates)

1. Asphaltic cement 1.02 6.0

2 Coarse aggregate 2.58 52.0 55.3

3 Fine aggregates 2.72 34.6 36.8

4 Mineral filler 2.70 7.4 7.9

100.0 100.0

Calculate

(i) Bulk density of specimen by uncoated specimen

procedure and immersion test.

(ii) Bulk density of specimen from specimen dimensions.

(iii) Bulk density of specimen by paraffin coated sample

procedure.

(iv) Average specific gravity of the aggregates

(v) Maximum theoretical density

(vi) Bulk density as percent of maximum density

(vii) Percent voids in compacted mix

(viii) Percent volume occupied by asphaltic cement, coarse

aggregate, fine aggregates, mineral filler.

(ix) Percentage volume of voids in mineral aggregate

(VMA).

(x) Percent aggregate voids filled with asphalt.

Page 28: Cec 204 Practical

28

Solution:

(i) Bulk density of specimen by uncoated specimen

immersed in water

W

W - Wsw

1174.74

1174.4 – 668.4

1174.4

506.3 = 2.320gm/cc

(ii) Bulk density from dimensions of specimen

= 1174.4

π x 10.16 x 10.16 x 6.20

4

= 2.337

(iii) Bulk density from paraffin coated specimen

WSA

WSA1

– WSW1

– ( WSA1

–WSA)

GP

= 1174.4

1220.9 – 664.4 – (1220.9 – 1174.4)

0.9

= 1174.4/505.2

= 2.325

(iv) Average specific gravity

Gag = Wag

Wca + Wfa + Wmf

Gca Gfa Gmf

= 100

55.3 + 36.8 + 7.9

2.58 2.72 2.70

(v) Maximum Theoretical density

W

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29

Wac + Wag

Gac Gag

= 1174.4

0.06 x 1174.4 + 0.94 x 1174.4

1.02 2.64

= 2.41gm/cc

(vi) Bulk density as percent of max theoretical density

= 2.32 x 100 = 96.3%

2.41

(vii) Percentage voids in compacted mix

% V = V – Vac - Vca - Vfa - Vfm x 100

V

= 1174.4 - 1174.4 x 0.06 - 1174.4 x 0.052

2.32 1.02 2.58

= 1174.4 x 0.346 - 1174.4 x 0.074

2.72 2.70

_____________________________ x 100

1174.4

2.32

= 3.7%

This is also given by

100 - Ɣm x 100

Ɣm1

100 – 2.32 x 100

2.41

100 – 96.3 = 3.7%

(viii) Percent volume occupied by constituents

% Vac = 6.00 x 2.32 = 13.7%

1.02

% Vca = 52.0 x 2.32 x 100 = 46.8%

2.58

% Vfa = 34.6 x 2.32 = 29.5%

2.72

% Vmf = 7.4 x 2.32 = 6.3%

2.70

% Vmf = 94.0 x 2.32 = 82.6%

2.64

Page 30: Cec 204 Practical

30

(ix) Percent volume of voids in mineral aggregate

(VMA)

= 100 - % weight of aggregate x W

Gag x V

100 – 0.94 x 1174.4 x 2.32

2.64 x 1174.4

= 100 – 82.6

= 17.4%

(x) Percent of aggregate voids filled with Asphaltic

concrete

= Percent of asphaltic cement in mix x 100

Percent of voids in mineral aggregate

= 13.7 x 100 = 78.7%

17.4

Page 31: Cec 204 Practical

31

WEEK 13

EXPERIMENT NO.12: DESIGN OF TRIAL MIX OF PLASTIC CONCRETE

CLASS ACTIVITY: A specimen of asphaltic concrete has a height of 6.20cm and a

diameter of 10.16cm, the weight of the compacted specimen

(uncoated) in air is 1174.4gms and in water, the weight is

668.4gms. When coated with paraffin, its weight in air is

1220.9gms and its weight when immersed in water is

664.4gms. The specific gravity of paraffin is 0.90. The analysis

of the specimen yielded the following:

S/No Material Specific

gravity

Mix composition

(% by weight of

total mix)

Aggregate

composition (%

by weight of total

aggregates)

1. Asphaltic cement 1.02 6.0

2 Coarse aggregate 2.58 52.0 55.3

3 Fine aggregates 2.72 34.6 36.8

4 Mineral filler 2.70 7.4 7.9

100.0 100.0

Calculate

(xi) Bulk density of specimen by uncoated specimen

procedure and immersion test.

(xii) Bulk density of specimen from specimen dimensions.

(xiii) Bulk density of specimen by paraffin coated sample

procedure.

(xiv) Average specific gravity of the aggregates

(xv) Maximum theoretical density

(xvi) Bulk density as percent of maximum density

(xvii) Percent voids in compacted mix

(xviii) Percent volume occupied by asphaltic cement, coarse

aggregate, fine aggregates, mineral filler.

(xix) Percentage volume of voids in mineral aggregate

(VMA).

(xx) Percent aggregate voids filled with asphalt.

Page 32: Cec 204 Practical

32

Solution:

(i) Bulk density of specimen by uncoated specimen

immersed in water

W

W - Wsw

1174.74

1174.4 – 668.4

1174.4

506.3 = 2.320gm/cc

(ii) Bulk density from dimensions of specimen

= 1174.4

π x 10.16 x 10.16 x 6.20

4

= 2.337

(iii) Bulk density from paraffin coated specimen

WSA

WSA1

– WSW1

– ( WSA1

–WSA)

GP

= 1174.4

1220.9 – 664.4 – (1220.9 – 1174.4)

0.9

= 1174.4/505.2

= 2.325

(iv) Average specific gravity

Gag = Wag

Wca + Wfa + Wmf

Gca Gfa Gmf

= 100

55.3 + 36.8 + 7.9

2.58 2.72 2.70

(v) Maximum Theoretical density

W

Page 33: Cec 204 Practical

33

Wac + Wag

Gac Gag

= 1174.4

0.06 x 1174.4 + 0.94 x 1174.4

1.02 2.64

= 2.41gm/cc

(vi) Bulk density as percent of max theoretical density

= 2.32 x 100 = 96.3%

2.41

(vii) Percentage voids in compacted mix

% V = V – Vac - Vca - Vfa - Vfm x 100

V

= 1174.4 - 1174.4 x 0.06 - 1174.4 x 0.052

2.32 1.02 2.58

= 1174.4 x 0.346 - 1174.4 x 0.074

2.72 2.70

_____________________________ x 100

1174.4

2.32

= 3.7%

This is also given by

100 - Ɣm x 100

Ɣm1

100 – 2.32 x 100

2.41

100 – 96.3 = 3.7%

(viii) Percent volume occupied by constituents

% Vac = 6.00 x 2.32 = 13.7%

1.02

% Vca = 52.0 x 2.32 x 100 = 46.8%

2.58

% Vfa = 34.6 x 2.32 = 29.5%

2.72

% Vmf = 7.4 x 2.32 = 6.3%

2.70

% Vmf = 94.0 x 2.32 = 82.6%

2.64

Page 34: Cec 204 Practical

34

(ix) Percent volume of voids in mineral aggregate

(VMA)

= 100 - % weight of aggregate x W

Gag x V

100 – 0.94 x 1174.4 x 2.32

2.64 x 1174.4

= 100 – 82.6

= 17.4%

(x) Percent of aggregate voids filled with Asphaltic

concrete

= Percent of asphaltic cement in mix x 100

Percent of voids in mineral aggregate

= 13.7 x 100 = 78.7%

17.4

Page 35: Cec 204 Practical

35

WEEK 14 TO 15

EXPERIMENT NO.14: STUDENTS TO BE TAKEN TO ROAD

CONSTRUCTION SITE

AIM: To identify different types of construction equipment and to see

the organization of site works.

OBJECTIVE: Know the uses of the equipment and to be aware of the

organizations of a site, together with the responsibility of the

staff.

REPORT: Students will be expected to write reports on different types of

construction equipment including diagrams and sketches seen

on site.

RESULT: a comprehensive report to be written, not less than 1000 words

and to be submitted 2 weeks after site visitation.

CONCLUSION: To be assessed by the lecturer.