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PART A:
EQUIPMENT
1. balance sensitive to 0.1 gram
2. Gilson Shaker: #4 and #8 screens and pan (the #4 and #8 U.S. Standard sieves
and pans may also be required)
3. scoops, spoons, spatulas
4. batch pans (with workstation numbers labelled on sides)
5. three plastic pails for sieved stock aggregate
6. one loaf tin for total mineral filler requirement
PROCEDURE
1. In the week prior to this lab session, use a trial and error approach on the
computer to arrive at a blend (proportions) of the coarse and fine aggregates and
mineral filler that produces a gradation curve that is as close to the midpoints
between the upper and lower limits of the grading spec as possible. The gradations
evaluated in the sieve analysis lab will be used to arrive at these proportions. These
blends should have been submitted to the instructor as an interim report prior to
this lab.
2. It is estimated that a total of 32 kg of aggregate would have to be sieved in
order to produce enough stock to produce twenty-two 1200 gram batches of
aggregate.
The mineral filler is NOT to be sieved but weighed out directly into the 22
batch tins.
The coarse and fine aggregate are sieved on the Gilson shaker in two halves: the
blending chart produced by the computer spreadsheet gives the amounts of each
type of aggregate to sieve to produce 32 kg of the blend. These weights should be
halved (and the mineral filler excluded) so as not to blind either of the screens.
For example, if the chart calls for 16.32 kg of coarse (CA) and 14.40 kg of fine (FA)
aggregate, weigh out 8.16 kg of CA and 7.20 kg of FA, place in the Gilson and sieve
on the #4 and #8 screens for 5 minutes. Then empty the material retained on the
screens and pan into the 3 stock pails. Then sieve another 8.16 kg of CA and 7.20
kg of FA as before, emptying the different sized material into their respective
stock pails.
3. Using the batch masses given in the last column of the blending chart produced
by the computer spreadsheet, weigh out the required amounts of each stock
material and place in each of the 22 batch tins in the following order:
First: mineral filler
Second: Gilson pan stock
Third: Gilson #8 stock
Lastly: Gilson #4 stock
4. Since the tins will be nested for storage and preheating, this ensures that the
material that would be most likely to be picked up by a nested tin is furthest away
from the top of the aggregate.
If one size of sieved stock runs out before all the batches are produced, the #4
and #8 U.S. Standard sieves and pans can be used to sieve small amounts rather
than waiting for the Gilson. If, for example, it is estimated that one more kilogram
of mixed aggregate would suffice, then, based on the previous example proportions,
16.32/32 or 0.51 kg of CA and 14.40/32 or 0.45 kg of FA should be sieved on the
#4 and #8 sieves and pan.
5. When all 22 batches have been weighed out they should be nested (stacked) in
fours or fives (based on the shelf space available) and then stored on the shelf
designated for your group.
6. Using the bulk specific gravities posted by the instructor for the coarse and fine
aggregates and the mineral filler, apply the proportions used to blend the aggregate
to calculate the bulk specific gravity of the blended aggregate, Gsb on Datasheet
25. Also enter the specific gravity of the asphalt to be used in the subsequent mix
calculations.
PART B:
EQUIPMENT
1. asphalt kettle and balance sensitive to 0.1 gram
2. mechanical mixer and metal mixing bowl
3. large mixing spoon and spatula
4. hot water bath and 2 sets of compaction mould assemblies (base, mould, collar)
6. compaction hammer and hot plate
7. compaction pedestal and mould holder
8. vinyl gloves and padded oven gloves
9. paper filter disks and keel (coloured wax crayon)
10. cold water bath (pail with snow/ice in water)
11. arbour press
12. large loose mix trays (2)
0.045 =
Mb
1200 + Mb
Mb =
54.0
= 56.4
0.955
2. The batches of aggregate mixed in the preceding session should have been heated
in the ovens to a temperature between 177 and 190 C prior to your arrival. The
asphalt in the kettle should be between 121 and 138 C. The procedure described
hereafter is repeated for each specimen. Efficiency is of the essence as the mix
must be at or above a temperature of 107 C when the mix is compacted. There is
no time to stand around discussing the weekends exploits! Each member of the
group should be assigned a task and be aware of the sequence of activities. This
means every participant should be familiar with these procedures BEFORE entering
the lab to perform them!
3. The mixing bowls must be kept in the oven when not in use. Similarly, the mould
assemblies should be kept in the water bath until required and returned
immediately after use and the compaction hammers must also be kept on the hot
plate when not in use. Everything that comes into contact with the asphalt mix
must be kept above the compaction temperature of 107 C. If the mix drops below
this temperature before compaction, the mix must be discarded.
4. The contents of an aggregate tin are placed in a mixing bowl and stirred
thoroughly, placed on the balance or scale, a crater is formed in the centre of the
aggregate and the balance (scale) is tared (set to 0).
5. The required weight of asphalt cement is added from the kettle. To avoid adding
too much, use a piece of heavy paper to intercept the asphalt cement stream when
the required weight is displayed. Since the stream can be controlled by a valve,
start to close the valve when the weight is within a couple of grams. If too much is
added, remove some by dipping the paper into the crater where the majority of the
asphalt cement has collected being careful not to remove any aggregate.
6. Quickly mix on the mechanical mixer until the asphalt cement is uniformly
distributed (no light coloured material, i.e., uncoated aggregate).
6
7. When the mixing is almost complete, one member of the group wearing the vinyl
gloves should remove and assemble a mould assembly on the bench top. A filter
paper disk should be placed in the mould before spooning the mix into the mould.
Spade the mixture vigorously 15 times around the perimeter and 10 times over the
interior. This moves the coarser material to the inside and the fines to the outside
to ensure a better shaped specimen. Remove the collar and smooth the top to a
slightly rounded shape.
Place another disk of filter paper on top, replace the collar and quickly insert the
mould assembly into the holding frame on the compaction pedestal.
8. Apply 50 blows with the compaction hammer, keeping the face of the hammer
parallel to the base plate. This can only be done by holding the hammer vertically,
so someone in the group should observe and ensure that this happens. The hand
that lifts the weight on the hammer should have a protective mitt (not a vinyl glove)
just in case that hand reaches the bottom of the hammer before the weight does.
This does happen, quite a lot actually.
9. Remove the collar, invert the mould on the base, replace the collar and apply
another 50 blows with the hammer. The hammer should be set on the hot plate
while the mould is being inverted.
10. Remove the collar and base, remove the filter paper from the specimen and place
the mould and specimen in the cold water bath until it is firm enough to be
extruded, without distortion, in the arbour press. This is usually when it feels
warm (not hot) while being held in your unprotected hands.
11. After extrusion in the arbour press, record the group number, asphalt content
and trial (e.g., 8-4.5B would be group eights second (B) trial at an asphalt content
of 4.5%) on the side of each specimen. This is done using the piece of yellow or red
keel supplied. As the specimen will still be a bit warm, this identification will
probably fade as the specimen cools. This ID should be touched up again before
storing.
The three trials for each asphalt content should be stacked and stored in the
designated shelf for your group once completed and cooled. It is recommended to
start with 4.5% AC and complete all three trial specimens (A, B and C) before going
on to 5.0% and so on. One member of the group should be in charge of keeping
7
track of the specimens to avoid unnecessary repetition (doing four trials for one
asphalt content instead of just three).
13. Dont even think of leaving until all the utensils, mixing bowls, mould assemblies,
asphalt decanting areas and water baths have been cleaned (Varsol is used to
remove asphalt from utensils). The cleanup should only take about half and hour if
everyone pitches in and helps.
PART C:
4. Check the Gmb values for outliers within each asphalt content. Datasheet 25
should be completed before arriving at this lab as the maximum possible Gmm
values for each asphalt content are recorded thereon and these provide a check
as they should be significantly higher than the Gmb values determined. If any
individual Gmb within one asphalt content group differs from the group average by
more than 0.015, the Gmbs must be verified by recalculation and if correct, then
each specimen within the group must be reweighed. If the specimen Gmb remains
more than 0.015 from the mean then the group mean Gmb must exclude this value.
If the specimens have been manufactured consistently and weighed correctly, the
Gmb values should agree reasonably well within each asphalt content.
5. At this point in the process it is possible (and recommended) to determine the
VMA of each specimen using the average specific gravity of the aggregate, Gsb
calculated on datasheet 25.
1. Take the 5% AC loose mix on the tray stored in the cupboard in Part B and
loosen any particles adhering to the tray and to each other. If there are any
significant sized chunks of mix make one last attempt to reduce them to the
required size.
2. Tare the scale to zero with the hanging basket submerged in the water barrel.
10
3. Place the clean and empty pycnometer in the basket and wipe the inside and
outside of the pycnometer while it is submerged to remove any air bubbles.
4. After the reading stabilizes, determine the mass of the pycnometer in water to
0.1 gram and record it on the master datasheet and on datasheet 26 as Mpw.
5. Remove the pycnometer and dry it off, making sure it is clean and dry (inside
and out).
6. Tare the pycnometer to zero at the weigh station, then, carefully pour the loose
mix into the pycnometer until a mass of about 1000 grams is collected. Read
this mass to the nearest 0.1 gram and record it on the master datasheet and on
datasheet 26 as Mmm.
7. Carefully insert the pycnometer into the water barrel and admit enough water
to cover the entire sample of loose mix (about full) and then remove and dry
the outside of the pycnometer.
8. Attach a lid with vacuum hose to the pycnometer and vacuum for 15 2 minutes.
Agitate the pycnometer vigorously every 2 minutes.
9. After vacuuming out the air from the sample and removing the vacuum lid,
tare the scale to zero again with the hanging basket submerged in the water
barrel, carefully immerse the pycnometer in the water barrel as before and
set it into the submerged basket, taking care to wipe any bubbles from the jar
surface without touching the sample.
10. After the reading stabilizes, determine the mass of the pycnometer and sample
in water to 0.1 gram and record it on the master datasheet and on datasheet 26
as Mpws.
11. The maximum specific gravity, Gmm should be determined IMMEDIATELY
(before doing anything else). If the Gmm value obtained is less than any of the
Gmb values at that asphalt content or greater than the maximum possible Gmm
value tabulated at that asphalt content on Datasheet 25, then something is
wrong and another trial to determine Gmm will have to be made in Part D. The
Gmm should decrease as asphalt content increases. This fact should also be used
to rationalize the validity of Gmm values determined.
11
PART D:
12
5. The Marshall Stability is the load in Newtons at which the specimen failed,
adjusted, if necessary, for the volume of the specimen. The load ring constant on
the Marshall tester is multiplied by the recorded load dial reading to produce the
Marshall Stability in Newtons. The load at failure in Newtons on the Versatester
can be read directly from the machine dial.
6. The Marshall flow is the deformation (change in diameter) of the specimen at the
time of failure. To obtain this reading, someone in the group must be watching the
strain dial and noting the reading when failure occurs. The person following the
load dial should say Now when the maximum load (failure) is reached. The
Marshall Flow is recorded in hundredths of an inch.
If the strain dial reading, for example, is noted as 22 units on a strain gauge with
100 divisions, each representing 0.01 of deformation, the Marshall Flow number is
22, whereas if each division represents 0.001 of deformation, the Flow number is
2.2.
If one full revolution of the strain dial divided into 100 divisions represents 1 mm
of deformation (i.e., each division represents 0.01 mm) and the reading at failure
was 559 units (five full revolutions and a final reading of 59), then the Marshall
Flow is 559/25.4 = 22.
On the face of each strain gauge the value of each division (1 div. = 0.01 or 0.01
mm) is printed. This should be noted before starting the testing so that the
proper units can be recorded for flow.
7. Each trial specimen (A, B and C) for the first two sets of asphalt content (5.0%
and 6.0%) should be saved in brownie tins (the three 5.0% AC specimens in one
and the three 6.0% AC specimens in the other). The member(s) designated to
perform the Maximum Specific Gravity, Gmm determinations (if necessary) should
begin their tasks as soon as the first specimens (5.0% AC ) become available. Since
the Gmm tests are not always successful, it might be wise to also save the 5.5% and
maybe even the 6.5 % specimens as well (just in case). These should be labelled
with the asphalt content on a piece of paper for identification because the
specimens look pretty much the same after testing. If Gmm values were
13
1. As soon as the specimens for the required %AC have been tested in the Marshall
Stability test, they should be broken apart in a mixing tray using trowels and by
hand. The specimens should be broken into particles no larger that a lima bean.
By quartering in the mixing tray, obtain a sample of between 900-1000 grams (3 x
(1200 + 63) /4 = 947).
2. Tare the scale to zero with the hanging basket submerged in the water barrel.
3. Place the clean and empty pycnometer in the basket and wipe the inside and
outside of the pycnometer while it is submerged to remove any air bubbles.
4. After the reading stabilizes, determine the mass of the pycnometer in water to
0.1 gram and record it on the master datasheet and on datasheet 26 as Mpw.
5. Remove the pycnometer and dry it off, making sure it is clean and dry (inside and
out).
6. Tare the pycnometer to zero at the weigh station, then, carefully pour the loose
mix into the pycnometer until a mass of about 900-1000 grams is collected. Read
this mass to the nearest 0.1 gram and record it on the master datasheet and on
datasheet 26 as Mmm.
14
7. Carefully insert the pycnometer into the water barrel and admit enough water to
cover the entire sample of loose mix (about full) and then remove and dry the
outside of the pycnometer.
8. Attach a lid with vacuum hose to the pycnometer and vacuum for 15 2 minutes.
Agitate the pycnometer vigorously every 2 minutes.
9. After vacuuming out the air from the sample and removing the vacuum lid, tare
the scale to zero again with the hanging basket submerged in the water barrel,
carefully immerse the pycnometer in the water barrel as before and set it into
the submerged basket, taking care to wipe any bubbles from the jar surface
without touching the sample.
10. After the reading stabilizes, determine the mass of the pycnometer and sample in
water to 0.1 gram and record it on the master datasheet and on datasheet 26 as
Mpws.
11. If the Gmm value obtained is less than any of the Gmb values at that asphalt
content or greater than the maximum possible Gmm value tabulated at that asphalt
content on Datasheet 25, then something is wrong.
At this point, since nothing has been discarded, the Gmm test could be repeated,
repeated with a different quarter of the sample or that asphalt content could be
abandoned in favour of another asphalt content (e.g., 5.5% or 6.5 %).
The Gmm should decrease as asphalt content increases. This fact should also be
used to rationalize the validity of Gmm values determined.
15
PART E:
I.
DATASHEET 24
This datasheet summarizes the sieving results from lab 1 and the blended
gradations, including the evaluation of grading using U.S.C. criteria and the Nominal
Maximum Particle Size as defined by the Asphalt Institute and by O.P.S.
II.
DATASHEET 25
The purpose of this datasheet is to determine the bulk specific gravity and
absorption capacity of the blended aggregate, Gsb and to document the specific
gravity of the asphalt cement, Gb. THREE DECIMAL PLACES are required for all
specific gravity values. Rounding to lower precision will result in errors in the mix
calculations.
PCA
GCAb
PFA
GFAb
16
PMF
GMFb
The total bulk volume of blended aggregate, Vsb would then be:
Vsb =
P
P
PCA
+ FA + MF
GCAb GFAb GMFb
Given that PCA + PFA + PMF = 100 grams, the bulk specific gravity of the blended
aggregate, Gsb would then be:
PCA + PFA + PMF
Gsb =
P
P
PCA
+ FA + MF
GCAb GFAb GMFb
where
rate at which the blended aggregate can absorb asphalt, Pbamax, which is estimated
using the following formulation:
1
1
Pbamax = Gb
G
G
sa
sb
where
III.
DATASHEET 26
2. The bulk specific gravity of the compacted mix, Gmb is calculated as follows:
Gmb =
where
Mmb
Vmb w
19
Msb = Mmb Mb
where
Msb = mass of aggregate in the specimen (grams)
Mmb = mass of the specimen in air (grams)
Mb = mass of asphalt cement in the specimen (grams)
3. The volume of asphalt cement in each specimen, Vb is calculated as follows:
Vb =
where
Mb
Gb w
Msb
Gsb w
6. The percent voids in the mineral aggregate, VMA is based on the bulk volume, Vmb:
VMA =
where
Vvma
100%
Vmb
21
Mmm
Mmm + Mpw Mpws
where
Gmm = maximum specific gravity of the voidless mix
Mmm = mass of loose mix sample (grams)
Mpw = mass of the pycnometer and basket in water (grams)
Mpws = mass of pycnometer + sample + basket in water (grams)
22
Mmb
Gmm w
where
Vmm = volume of the voidless mix (cm3)
Mmb = mass of the specimen in air (grams)
Gmm = maximum specific gravity of the voidless mix
w = the density of water (g/cm3)
2. The effective volume of the mineral aggregate, Vse is calculated as follows:
Vse = Vmm Vb
where
Vse = effective volume of the mineral aggregate (cm3)
Vmm = volume of the voidless mix (cm3)
Vb = volume of asphalt cement in each specimen from step 3 in VMA calc. (cm3)
3. The volume of air in the compacted mix, Va is then found:
Va = Vmb Vmm
where
Va = volume of air in the compacted mix (cm3)
Vmm = volume of the voidless mix (cm3)
Vmb = bulk volume of the specimen (cm3)
23
Mba
100%
Msb
where
Pba = percent asphalt absorbed by the aggregate in the mix
Mba = mass of asphalt absorbed by aggregate in the compacted mix (grams)
Msb = mass of mineral aggregate in the specimen (grams)
7. The effective specific gravity of the aggregate, Gse is then found as follows:
Gse =
Msb
Vse w
where
Gse = effective specific gravity of the blended mineral aggregate in the mix
Msb = mass of mineral aggregate in the specimen (grams)
Vse = effective volume of the mineral aggregate (cm3)
w = the density of water = 1.0 g/cm3
24
Va
100%
Vmb
where
Pa = percent air voids in the compacted mix
Va = volume of air in the compacted mix (cm3)
Vmb = bulk volume of the specimen (cm3)
specific gravity, Gse of the aggregate from A above is used to find the percent air
voids, Pa, the percent asphalt absorbed, Pba and to estimate the maximum specific
gravity, Gmm.
1. First, find the effective volume of the mineral aggregate, Vse using the
Msb
Gse w
where
Vse = effective volume of the mineral aggregate (cm3)
Msb = mass of mineral aggregate in the specimen (grams)
Gse = average effective specific gravity of the blended mineral aggregate
w = the density of water (g/cm3)
2. The volume of the voidless mix, Vmm is then calculated as follows:
Vmm = Vse + Vb
where
Vmm = volume of the voidless mix (cm3)
Vse = effective volume of the mineral aggregate (cm3)
Vb = volume of asphalt cement in each specimen from step 3 in VMA calc. (cm3)
25
Mba
100%
Msb
26
7. The maximum specific gravity of the voidless mix, Gmm is then estimated as
follows:
Gmm =
Mmb
Vmm w
where
Gmm = maximum specific gravity of the voidless mix
Mmb = mass of the specimen in air (grams)
Vmm = volume of the voidless mix (cm3)
w = the density of water = 1.0 g/cm3
It should be noted that the Gmm should decrease with asphalt content and be
greater than the bulk specific gravity, Gmb calculated for each specimen at the
asphalt content under scrutiny. These considerations can be used to determine
whether or not the properties of each trial specimen are rational and consistent.
8. The percent air voids, Pa in the compacted mix is then calculated:
Pa =
Va
100%
Vmb
where
Pa = percent air voids in the compacted mix
Va = volume of air in the compacted mix (cm3)
Vmb = bulk volume of the specimen (cm3)
where
VFA = percentage of the volume of voids in the mineral aggregate filled with
asphalt cement in each specimen
Vmm = volume of the voidless mix (cm3)
Vsb = volume of mineral aggregate in each specimen (cm3)
Vvma = volume of voids in the mineral aggregate (cm3)
27
IV. DATASHEET 27
Datasheet 27 is a summary of all the calculations on the 6 copies (one for each
asphalt content) of datasheet 26. The averages for each parameter will be used to
generate plots of each parameter versus percent asphalt content.
The values being averaged must be reasonably close to each other numerically but
they must also make sense in terms of relationships between parameters:
a) The maximum specific gravities, Gmm should be higher than the bulk specific
gravities, Gmb for each asphalt content. The maximum specific gravity, Gmm
should decrease as asphalt content increases.
b) The percent asphalt absorbed, Pba should not exceed the maximum possible
asphalt absorption capacity of the blended aggregate, Pbamax.
c) The Gmb and Adjusted Marshall Stability values usually result in a maximizing
shaped curve.
d) The VMA values usually range between 10 and 20 percent and show a
minimizing shaped curve.
e) The Marshall Flow values usually increase with asphalt content.
f) The percent air voids, Pa, usually decreases with increasing asphalt content.
g) The VFA values should increase with asphalt content, but not past 100%!
The calculated values for each specimen should be scrutinized for logical and
statistical viability. Values that are logically non-viable (eg., negative) should be
stroked out with a horizontal line in the summary table of Datasheet 27. Statistical
outliers should be crossed out (X) as in lab 2. The average value of each parameter
for each asphalt content should then be based only on the viable values.
In some instances, the calculated parameters might seem reasonable, but the
Marshall Stability and flow results (for example) may seem unreasonable for one
particular asphalt content. This could be the result of leaving the specimens in the
water bath for too long or not long enough or inconsistent water bath temperature.
Sometimes one of the specimens is not tested correctly (missed the maximum load
28
dial reading or flow dial reading at maximum load). If specimens are rejected due to
irregularities in Marshall testing, parameters such as Gmb, Gmm, VMA and Pa may still
be valid and need not automatically be excluded from the analysis. Again, any values
rejected must be documented in the report.
29
VI.
REPORT
top left: bulk specific gravity, Gmb versus percent asphalt content,
b)
c)
d)
e)
f)
g)
3. Datasheets 24 (1), 25 (1), 26 (6) and 27 (1) should be properly completed. Any
rejected data on datasheet 27 should be clearly indicated as described in
Section IV above.
a)
30
VII.
Mmm
Mpw
Mpws
Msb
Pa
Pb
Pba
Vsb
Vse
31