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TECHNICAL PAPER
INTRODUCTION
Alkali-silica reaction (ASR) is one of the utmost recognized harmful phenomena in concrete structures, and has
been a major distress since its discovery by Stanton (1942) in
the late 1930s. ASR occurs between the reactive silica or silicates present in aggregates with certain mineralogy and the
alkalis (mainly coming from portland cement) in concrete.
The resulting product, named alkali-silica gel, expands in
the presence of sufficient moisture, causing cracks, a loss of
mechanical properties, and serviceability-related problems
in portland cement concrete (Bach et al. 1993; Stark et al.
1993; Lger et al. 1996). The potential reactivity of aggregates depends on aggregate mineralogy (Stark et al. 1993;
Leming et al. 1996; Islam 2010; Islam and Akhtar 2013),
atomic structure (Leming et al. 1996), physico-chemical
compositions (Pietruszczak 1996; Tambelli et al. 2006),
grain size (Hobbs 1988; Broekmans 1999; achlov 2013),
porosity (Hobbs 1988), degree of crystallinity (Folliard
et al. 2005; achlov 2013), solubility of silica in high-pH
concrete pore solution (Swamy 1992; Broekmans 1999;
Folliard et al. 2005), and amount of reactive silica present
in aggregate (Swamy 1992; Broekmans 1999; Folliard et al.
2005). Though a very small amount of reactive silica can
produce ASR-related damages (Swamy 1992), the quantity
differs depending on aggregates reactive minerals and rock
type (ACI Committee 221 1998).
ASTM C1260, commonly known as the accelerated mortar
bar test (AMBT), is one of the most widely used methods
to assess the alkali silica reactivity (ASR) of aggregates
ACI Materials Journal/January-February 2016
13
Table 1Identification, chemical composition, rock type, and potential ASR reactivity of trial aggregates
Chemical composition, %
Aggregate
ID
SiO2
Al2O3
Fe2O3
CaO
MgO
Na2O
K2O
Loss on
ignition
Rock type
Potential ASR
Field performance
A-1
13.50
0.40
0.29
32.55
13.09
0.03
0.14
39.4
Dolomite-limestone
Reactive
N.R.
A-2
63.09
11.50
3.48
6.92
1.97
2.34
3.28
6.43
Dacite
Reactive
Reactive
A-3
60.82
15.89
5.37
4.34
2.49
3.57
3.73
2.14
Andesite
Reactive
Reactive
A-4
68.00
15.48
2.86
1.14
0.94
4.52
5.40
0.63
Dacite
Reactive
Reactive
A-5
59.33
17.15
5.83
5.30
2.54
3.76
2.68
1.83
Andesite
Reactive
Reactive
A-6
52.50
18.45
8.35
8.36
4.59
3.74
1.22
0.98
Basaltic-andesite
Reactive
Reactive
14
RESEARCH SIGNIFICANCE
This study serves as an extension to the past research
studies by: a) proposing prediction models of using the
SiO2(eq), CaOeq, and CaOeq/SiO2(eq) of total cementitious
materials to determine the minimum dosage of Class F fly
ash needed to inhibit the ASR-induced expansion below
the recommended failure limits at 14, 28, and 56 days; and
b) verifying the validation of the proposed models on the
experimental data of the previous studies consisting of eight
aggregates having different mineralogy, two types of portland cements, and six types of Class F fly ashes having a
wide range of chemical compositions. Finally, a detailed
statistical analysis was performed to support the findings.
EXPERIMENTAL PROGRAM
The reactive aggregates used in this study were acquired
from six different quarries. The identification, percent chemical composition (rock type), and potential reactivity of each
aggregate are shown in Table 1. The chemical compositions
of ASTM Type V portland cement used in this study were:
21% SiO2, 3.6% Al2O3, 3.4% Fe2O3, 63.1% CaO, 4.7% MgO,
0.84% Na2Oeq, 2.6% SO3, and 1.3% loss on ignition (LOI).
Class F fly ash consisted of 57.8% SiO2, 21.7% Al2O3, 5.1%
Fe2O3, 7.4% CaO, 0.30% Na2Oeq, and 0.2% LOI was also
used as sole secondary cementitious material.
Table 2 shows the mixture constituents of mortar bars,
conformed to the requirements ASTM C1260 (2007) and
C1567 (2007), prepared with various dosages (0, 15, 20, 25,
and 30%) of Class F fly ash as a partial replacement of portland cement by weight. The SiO2(eq), CaOeq, and the ratio
of CaOeq and SiO2(eq) of the total cementitious materials in
the studied mortar bars are also presented in Table 2. Four
mortar bar specimens were prepared from each reactive
aggregate type and each dosage of Class F fly ash content.
The mortar bars were mixed in accordance with the requirements of ASTM C305, and they were molded within a total
elapsed time of less than 2 minutes and 15 seconds. After
24 hours of moist curing, the bars were demolded and initial
readings were taken. The bars were then stored in water at
80C (176F) for 24 hours, after which the zero readings
were recorded. Afterward, the specimens were immersed in
1N NaOH solution in an air-sealed plastic container maintaining a temperature of 80C (176F). Additional readings
were taken at 3, 6, 10, and 14 days, and one reading per week
until the immersion age of 98 days.
ACI Materials Journal/January-February 2016
Table 2Mixture constituents of mortar bars prepared with various dosages of Class F fly ash
Test
Fly ash, %
Graded aggregate, g
w/c*
Portland
cement, g
ASTM C1260
ASTM C1567
Class F
fly ash, g
SiO2(eq), %
CaOeq, %
CaOeq/SiO2eq
2310.0
0.47
1026.7
0.0
24.40
71.84
2.94
15
2310.0
0.47
872.7
154.0
31.61
62.27
1.97
20
2310.0
0.47
821.3
205.4
34.02
59.07
1.74
25
2310.0
0.47
769.9
256.7
36.42
55.88
1.53
30
2310.0
0.47
718.5
308.0
38.83
52.69
1.36
28-day
56-day
Aggregate
ID
14-day*
(0.10%)
(0.28%)
(0.33%)
(0.47%)
(0.48%)
A-1
15
15
20
20
20
A-2
15
15
15
15
15
A-3
25
20
25
25
25
A-4
20
15
15
15
20
A-5
25
25
30
30
30
A-6
25
25
30
30
30
Failure criteria proposed by Hooton (1991, 1995) and Hooton and Rogers (1993).
Fig. 3Reduction in expansion of mortar bars treated with: (a) 15%; and (b) 30% Class F fly ash dosages.
capable of inhibiting ASR-related expansions of the mortar
bars immersed in the solution for 28 and 56 days, whereas
the amount was insufficient to reduce the mortar expansion
below the expansion limit of 0.10% at 14 days. Table 3 also
shows that the 28- and 56-day failure criteria resulted in a
good agreement on the ASR classifications of the trial aggregates when treated with various dosages of Class F fly ash.
Because the alkali-silica reactivity of aggregate depends on
a number of factors, it is recommended to use the maximum
required fly ash dosage in controlling the mortar expansion
of each reactive aggregate below the expansion limits of
0.10% at 14 days, 0.28% at 28 days, and 0.47% at 56 days.
As such, the extended failure limits of 0.28% at 28 days
and 0.47% at 56 days, proposed by Islam (2010), would be
used instead of the expansion limits (0.33% at 28 days and
0.48% at 56 days) recommended by Hooton (1991, 1995)
and Hooton and Rogers (1993).
Reduction in expansion of control mortar bars
treated with Class F fly ash
The effectiveness of Class F fly ash in suppressing the
control expansion of the selected reactive aggregates was
expressed in term of reduction in expansion (RIE) of the
untreated mortar bars prepared with the companion aggregate groups. The characteristic of the RIE of the mortar bars
prepared with 15 and 30% Class F fly ash dosages over the
test duration is shown in Fig. 3. As can be seen, the RIE at the
early age of 14 days was shown to be the highest, and then
gradually decreased with an increase in the test duration. For
each fly ash replacement, the RIE decreased rapidly with an
increase in test duration at lower fly ash content (15%) than
that obtained for the higher (30%) fly ash mortar bars. The
RIE of the specimens treated with 30% Class F fly ash over
the test duration of 98 days was fairly linear for all aggregate
groups (Fig. 3(b)) when compared to that of made with 15%
fly ash content (Fig. 3(a)). After approximately 3 months of
testing, the RIE became relatively constant, indicating that
the expansion rate of the fly ash specimens was similar to
that of the untreated mortar bars.
The 14-day RIE of the mortar bars made with the selected
reactive aggregates varied from 61.9 to 75.5% with an
average of 70.2% for the 15% fly ash, from 77.3 to 85.1%
with an average of 81.7% for the 20% fly ash, from 83.4 to
91.6% with an average of 88.0% for the 25% fly ash, and
from 87.4 to 96.3% with an average of 92.5% for the 30%
16
(4)
(5)
(6)
Fig. 4Relationship between 14-day expansion of A-4 aggregate and: (a) SiO2(eq); (b) CaOeq; and (c) CaOeq/SiO2(eq) of total
cementitious materials.
a decrease of SiO2(eq) of total cementitious materials. The
expansion increased with an increase of CaOeq and CaOeq/
SiO2(eq) of total cementitious materials present in mortar
bars, as shown in Fig. 4(b) and (c), respectively. The trends
indicated an agreement with the findings obtained by the
past research investigations (Malvar and Lenke 2005, 2006).
Once the test duration was extended to 28 and 56 days, the
patterns of the data points of A-4 aggregate for the SiO2(eq),
CaOeq, and CaOeq/SiO2(eq) of total binding materials in the
mortar bar were found to be identical to that observed in
Fig. 4(a), (b), and (c), respectively. The expansion behavior
of the remaining five aggregates displayed a similar characteristic to that of the A-4 aggregate group. As such, the
typical relationships between the mortar expansions and the
SiO2(eq), CaOeq, and CaOeq/SiO2(eq) of total binding materials
in the mortar bars at the test durations of 14, 28, and 56 days
can be represented by linear regressions of Eq. (7), (8), and
(9), respectively
regression coefficients of ms and cs, the t-ratio of both regression coefficients, the standard error of the estimate, and the R2
and R2adj of Eq. (7) for each aggregate group were determined.
The results are documented in Table 4.
As can be seen in Table 4, the t-ratio of each regression
coefficient (ms and cs) was much greater than 1.0, which indicated that the both parameters are more significant to Eq. (7).
The coefficients of determination of Eq. (7) for all aggregate
groups (R2 = 85.2 to 99.5) implied that approximately 85 to
99% of the variability of dependent variable (mortar expansion) was explained by the linear model. Additionally, the
adjusted coefficient of determination (R2adj), another reliable
parameter for the model, was shown to be very close to the
R2 values, and the standard errors of the estimate (0.026 to
0.150) were very low. It indicates that the expansion data
of the investigated six reactive aggregates were nicely fitted
with Eq. (7).
The relationships between the mortar expansions and the
CaOeq and CaOeq/SiO2(eq) of total binding materials were also
fitted with Eq. (8) and (9), respectively. The values of mc,
cc, mc/s, and cc/s were determined for each aggregate group
during the test durations of 14, 28, and 56 days. Additionally,
the analysis of variance of Eq. (8) and (9) for each reactive
aggregate was also performed. The results obtained from
various statistical parameters of R2, R2adj, standard error of
the estimate, and Prob(F) showed that Eq. (8) and (9) were
shown to be a very good fit for experimental expansion data
and the CaOeq and the CaOeq/SiO2(eq) of total binding materials at 14, 28, and 56 days, respectively.
The coefficients of ms and cs of Eq. (7), mc and cc of
Eq. (8), and mc/s and cc/s of Eq. (9) were correlated with the
expansion of control mortar bars and the test durations of 14,
28, and 56 days. The regression equations that fit most with
the independent variables and the response variables of ms,
cs, mc, cc, mc/s, and cc/s were represented by Eq. (10) through
(15), respectively. As can be demonstrated, approximately
99.0%, 99.6%, 99.0%, 97.9%, 99%, and 91.7% of the independent variables (mortar expansion and test duration) were
explained by the coefficients of ms, cs, mc, cc, mc/s, and cc/s,
respectively. The adjusted coefficients of multiple determination (RadjR) were shown to be very close to measured R2,
and Prob(F) was shown to be 0.0000. These indicated that
Eq. (10) through (15) were well-fitted between the coefficients (ms, cs, mc, cc, mc/s, and cc/s) and the independent variables of control mortar expansion and test duration.
17
Table 4Coefficients and statistical significance of Eq. (7) for each aggregate for test durations of 14, 28,
and 56 days
Aggregate
ID
A-1
A-2
A-3
A-4
A-5
A-6
t-ratio
Parameters
Test duration,
days
Standard error
R2
R2adj
14
0.649
0.017
16.586
14.304
0.026
0.919
0.915
28
1.268
0.032
23.516
20.102
0.036
0.957
0.955
56
2.086
0.052
22.719
18.766
0.061
0.951
0.949
14
0.787
0.021
11.564
10.177
0.045
0.852
0.844
28
1.457
0.038
14.247
12.403
0.068
0.895
0.889
56
2.168
0.055
20.751
17.517
0.069
0.945
0.942
14
2.247
0.059
15.023
13.240
0.099
0.907
0.902
28
2.811
0.071
18.272
15.433
0.102
0.930
0.926
56
2.934
0.069
28.122
22.039
0.069
0.964
0.962
14
1.175
0.031
15.966
14.035
0.049
0.916
0.912
28
1.518
0.038
25.580
21.528
0.039
0.963
0.961
56
1.834
0.044
33.487
26.661
0.036
0.975
0.974
14
2.813
0.075
13.870
12.399
0.134
0.895
0.889
28
3.949
0.102
17.482
15.070
0.150
0.927
0.923
56
4.698
0.112
47.295
37.624
0.066
0.987
0.987
14
2.260
0.060
15.444
13.695
0.097
0.912
0.908
28
2.993
0.076
23.824
20.146
0.083
0.958
0.955
56
3.478
0.081
76.028
59.436
0.030
0.995
0.995
18
where Exp0%FA is control expansion (%); ms, mc, and mc/s are
the slopes of the linear regression lines of Eq. (7) through
(9), respectively; cs, cc, and cc/s are the intercepts of the linear
regression lines of Eq. (7) through (9), respectively; and T is
test duration, in days.
The minimum dosages of Class F fly ash content to
suppress alkali-silica reactivity using the CaOeq and
CaOeq/SiO2(eq) of total cementitious materials in mortar
bars was also evaluated using the similar procedures to that
obtained using the SiO2(eq) of total cementitious materials.
Tables 6 and 7 present the prediction of optimum Class F fly
ash content in the mortar bars to suppress ASR using the CaOeq
and CaOeq/SiO2(eq) of total cementitious materials at the test
durations of 14, 28, and 56 days, respectively. As can be seen in
Tables 5 through 7, a good agreement existed between the
required optimum Class F fly ash content evaluated by
experimental setting, and that predicted by the proposed
models using SiO2(eq), CaOeq and CaOeq/SiO2(eq) of total
cementitious materials present in the mortar bars at the ages
of 14, 28, and 56 days.
Figure 5 shows the percent difference between the
optimum experimental and analytical fly ash contents for
each reactive aggregates at the test durations of 14, 28, and
56 days. As can be seen, the variations in optimum Class F fly
ash content obtained from the experimental procedures and
the proposed analytical methods using three different chemical
compositions (SiO2(eq), CaOeq, and CaOeq/SiO2(eq)) of binding
materials were insignificant for each reactive aggregate and
test duration. The optimum experimental fly ash dosage that
ACI Materials Journal/January-February 2016
Table 5Prediction of optimum Class F fly ash content (SiO2(eq)) in mortar bars to suppress ASR using
SiO2(eq) of total cementitious materials
Aggregate
ID
A-1
A-2
A-3
A-4
A-5
A-6
Control
expansion, %
14
cs
Suppressive
expansion, %
Estimated
SiO2(eq)
Analytical fly
ash||, %
Experimental
fly ash, %
0.275
0.0190
0.7040
0.080
32.92
17.7
15.0
28
0.502
0.0312
1.2287
0.224
32.18
16.2
15.0
56
0.823
0.0463
1.9275
0.248
36.27
24.7
20.0
14
0.310
0.0222
0.8270
0.071
33.97
19.8
15.0
28
0.570
0.0367
1.4458
0.170
34.74
20.0
15.0
56
0.870
0.0500
2.0840
0.360
34.47
20.3
15.0
14
0.890
0.0606
2.2679
0.099
35.79
23.7
25.0
28
1.171
0.0723
2.8597
0.236
36.29
24.7
25.0
56
1.318
0.0738
3.0833
0.434
35.89
23.9
25.0
14
0.465
0.0319
1.1882
0.081
34.72
21.5
20.0
28
0.620
0.0385
1.5178
0.262
32.58
17.0
15.0
56
0.800
0.0450
1.8750
0.412
32.48
16.8
15.0
14
1.097
0.0746
2.7944
0.082
36.38
24.9
25.0
28
1.600
0.0984
3.9007
0.251
37.09
26.4
25.0
56
1.993
0.1112
4.6552
0.432
37.99
28.3
30.0
14
0.886
0.0603
2.2580
0.079
36.12
24.4
25.0
28
1.218
0.0751
2.9727
0.236
36.42
25.0
25.0
56
1.514
0.0847
3.5403
0.352
37.64
27.5
30.0
Mortar expansion, determined by experimental procedures, below failure limits of 0.10% at 14 days, 0.28% at 28 days, and 0.47% at 56 days.
(16)
(17)
19
Table 6Prediction of optimum Class F fly ash content (CaOeq) in mortar bars to suppress ASR using
CaOeq of total cementitious materials
Aggregate
ID
Control
expansion, %
14
A-1
A-2
A-3
A-4
A-5
A-6
cc
Suppressive
expansion, %
Estimated
CaOeq
Analytical fly
ash||, %
Experimental
fly ash, %
0.275
0.0143
0.7827
0.080
60.44
17.9
15.0
28
0.502
0.0235
1.2183
0.224
61.31
16.5
15.0
56
0.823
0.0348
1.7060
0.248
56.07
24.7
20.0
14
0.310
0.0168
0.9182
0.071
59.06
20.0
15.0
28
0.570
0.0276
1.4315
0.170
57.93
21.8
15.0
56
0.870
0.0377
1.8432
0.360
58.49
20.9
15.0
14
0.890
0.0457
2.4949
0.099
56.79
23.6
25.0
28
1.171
0.0545
2.8138
0.236
56.00
24.8
25.0
56
1.318
0.0556
2.7173
0.434
56.68
23.7
25.0
14
0.465
0.0240
1.3148
0.081
58.11
21.5
20.0
28
0.620
0.0290
1.5020
0.262
60.81
17.3
15.0
56
0.800
0.0339
1.6599
0.412
61.11
16.8
15.0
14
1.097
0.0562
3.0682
0.082
56.04
24.7
25.0
28
1.600
0.0742
3.8272
0.251
54.99
26.4
25.0
56
1.993
0.0837
4.0873
0.432
53.97
28.0
30.0
14
0.886
0.0455
2.4841
0.079
56.36
24.3
25.0
28
1.218
0.0566
2.9239
0.236
55.83
25.1
25.0
56
1.514
0.0638
3.1162
0.352
54.38
27.4
30.0
Mortar expansion, determined by experimental procedures, below failure limits of 0.10% at 14 days, 0.28% at 28 days, and 0.47% at 56 days.
(18)
For PC1+FA1
(28)
(29)
(30)
(19)
(20)
(21)
For PC1+FA2
(22)
(23)
(24)
For PC1+FA3
(25)
(26)
(27)
For PC1+FA4
20
Table 7Prediction of optimum Class F fly ash content (CaOeq/SiO2(eq)) in mortar bars to suppress ASR
using CaOeq/SiO2(eq) of total cementitious materials
Aggregate ID
A-1
A-2
A-3
A-4
A-5
A-6
mc/s*
cc/s
Suppressive
expansion,
%
0.275
0.1752
0.2514
0.080
1.89
18.0
15.0
28
0.502
0.2841
0.3318
0.224
1.95
16.8
15.0
56
0.823
0.4143
0.3937
0.248
1.55
24.4
20.0
14
0.310
0.2056
0.2952
0.071
1.78
20.0
15.0
28
0.570
0.3338
0.3902
0.170
1.68
22.0
15.0
56
0.870
0.4477
0.4255
0.360
1.75
20.6
15.0
14
0.890
0.5592
0.8069
0.099
1.62
23.1
25.0
28
1.171
0.6568
0.7701
0.236
1.53
24.7
25.0
56
1.318
0.6603
0.6288
0.434
1.61
23.3
25.0
14
0.465
0.2945
0.4236
0.081
1.71
21.3
20.0
28
0.620
0.3503
0.4095
0.262
1.92
17.5
15.0
56
0.800
0.4031
0.3830
0.412
1.97
16.5
15.0
14
1.097
0.6879
0.9935
0.082
1.56
24.2
25.0
28
1.600
0.8937
1.0494
0.251
1.45
26.2
25.0
56
1.993
0.9938
0.9482
0.432
1.39
27.4
30.0
14
0.886
0.5568
0.8034
0.079
1.58
23.8
25.0
28
1.218
0.6825
0.8004
0.236
1.52
25.0
25.0
56
1.514
0.7574
0.7217
0.352
1.42
26.9
30.0
Control
expansion, %
14
Estimated
SiO2(eq)
Mortar expansion, determined by experimental procedures, below failure limits of 0.10% at 14 days, 0.28% at 28 days, and 0.47% at 56 days.
Fig. 5Percent difference between experimental and analytical fly ash contents for each reactive aggregate at test durations
of: (a) 14 days; (b) 28 days; and (c) 56 days.
of 14 and 28 days. As can be shown, the proposed empirical
models of using the SiO2(eq), CaOeq, and CaOeq/SiO2(eq) of total
cementitious materials resulted in nearly identical outcomes
for each reactive aggregate, which showed a good alignment
with the findings obtained by experimental procedures.
To validate the three empirical models proposed in this
study, they were used to predict the optimum amounts of
Class F Fly ash in suppressing the mortar expansions of 14
reactive aggregate groups (six from this study, six from the
studies conducted by Touma [2000] and Touma et al. [2001],
and remaining two from the study conducted by Schwing
ACI Materials Journal/January-February 2016
Table 8Identification, mineralogy, source, and reactivity of aggregates used in previous studies
Studies
Touma
(2000),
Touma et al.
(2001)
Aggregate
ID
Aggregate mineralogy
Aggregate source
Reactivity
Field
performance
A2-WY
Rhyolite
Wyoming
Reactivity
Reactive
A4-ID
Idaho
Reactivity
Reactive
A6-NM
Rhyolite, andesite
New Mexico
Reactivity
Reactive
B4-VA
Virginia
Reactivity
N.R.
C2-SD
South Dakota
Reactivity
Reactive
E2-IA
Iowa
Reactivity
Innocuous
A1
Oregon
Reactivity
N.R.
A2
Texas
Reactivity
N.R.
Schwing
(2010)
Cememtitious materials
SiO2
Al2O3
Fe2O3
CaO
MgO
Na2Oeq
SO3
Loss on
ignition
Touma (2000),
Touma et al. (2001)
20.90
3.43
3.01
62.65
2.97
1.14
3.06
1.68
56.50
19.30
4.70
12.30
2.30
0.30
1.50
0.30
20.08
5.61
2.51
63.79
1.22
0.79
3.39
1.59
47.66
21.58
4.21
12.3
2.70
6.61
1.20
0.76
54.06
16.36
6.01
11.16
4.14
4.52
0.64
0.24
63.95
16.54
4.43
6.16
2.38
3.28
0.54
0.31
59.36
25.14
5.56
5.63
0.94
1.04
0.37
0.16
Schwing (2010)
Table 10Prediction of optimum Class F fly ash content of each reactive aggregate used in the studies
conducted by Touma (2000) and Touma et al. (2001)
Aggregate
ID
A2-WY
A4-ID
A6-NM
B4-VA
C2-SD
E2-IA
Test durations,
days
Control
expansion, %
Suppressive
expansion*, %
SiO2(eq)
CaOeq
CaOeq/SiO2(eq)
Experimental
fly ash dosage, %
14
0.245
0.050
21.1
21.0
19.7
20.0
28
0.370
0.140
19.0
18.9
18.3
20.0
14
0.790
0.100
24.2
24.2
22.4
20.0
28
0.950
0.220
24.7
25.0
23.6
20.0
14
0.910
0.120
24.1
24.0
22.2
20.0
28
1.120
0.270
24.4
24.7
23.3
20.0
14
0.150
0.030
21.0
21.1
19.7
20.0
28
0.280
0.060
24.7
25.4
24.0
20.0
14
0.170
0.040
20.0
19.8
18.7
20.0
28
0.300
0.090
21.7
22.0
21.0
20.0
14
0.420
0.060
23.4
23.4
21.7
20.0
28
0.620
0.100
27.0
27.7
26.0
20.0
Expansion of mortar bars treated with Class F fly ash below failure limits of 0.10% at 14 days and 0.28% at 28 days except for A4-ID aggregate.
compared to the optimum dosages of Class F fly ash determined by the experimental procedures.
Because the ASR of a reactive aggregate and its interactions with Class F fly ash depend on various factors, it
is recommended to use the analytical minimum dosage of
Class F fly ash that was sufficient to suppress the excess
22
Table 11Prediction of optimum Class F fly ash content of each reactive aggregate used in the study
conducted by Schwing (2010)
Aggregate
ID
Class F fly
ash ID
FA1
FA2
A1
FA3
FA4||
FA1
FA2
A2
FA3
FA4||
Test
durations, days
Control
expansion, %
Suppressive
expansion*, %
SiO2(eq)
CaOeq
CaOeq/SiO2(eq)
14
0.656
0.085
29.6
25.0
28.5
25.0
28
0.851
0.211
29.6
25.4
29.4
25.0
14
0.656
0.039
29.2
27.0
31.0
35.0
28
0.851
0.142
29.9
28.2
32.7
35.0
14
0.656
0.100
21.1
19.6
24.3
25.0
28
0.851
0.278
19.3
18.7
22.7
25.0
14
0.656
0.030
23.8
21.5
27.3
25.0
28
0.851
0.121
24.7
22.9
29.2
25.0
14
0.280
0.079
23.2
18.3
23.5
25.0
28
0.405
0.138
22.8
20.8
26.3
25.0
14
0.280
0.036
26.3
23.9
28.4
35.0
28
0.405
0.096
26.9
24.9
29.8
35.0
14
0.280
0.037
26.2
20.1
25.2
25.0
28
0.405
0.116
24.9
19.1
24.5
25.0
14
0.280
0.040
25.8
18.1
24.0
25.0
28
0.405
0.086
27.7
20.2
26.6
25.0
Expansion of mortar bars treated with Class F fly ash below failure limits of 0.10% at 14 days and 0.28% at 28 days.
Using Eq. (19), (20), and (21) for SiO2(eq), CaOeq, and CaOeq/SiO2(eq), respectively.
Using Eq. (22), (23), and (24) for SiO2(eq), CaOeq, and CaOeq/SiO2(eq), respectively.
Using Eq. (25), (26), and (27) for SiO2(eq), CaOeq, and CaOeq/SiO2(eq), respectively.
||
Using Eq. (28), (29), and (30) for SiO2(eq), CaOeq, and CaOeq/SiO2(eq), respectively.
*
CONCLUSIONS
1. The mortar expansion decreased with an increase in fly ash
content. The percent reduction in expansion of the fly-ash treated
mortar bars was highest at 14 days and gradually decreased with
an increase in test duration. Additionally, the reduction in expansion decreased more rapidly with an increase in test duration at
the lower fly ash content (that is, 15%) than that obtained for the
mortar bars made with higher fly ash dosage (that is, 30%).
2. For a few aggregates, the minimum experimental
Class F fly ash dosage to inhibit excessive ASR-induced
expansions below the 0.10% at 14 days proved to be effective
in reducing expansions below 0.28% at 28 days and 0.47%
at 56 days. However, for the most reactive aggregates, a
higher dosage of Class F fly ash was needed to suppress ASR
expansions at 28 and 56 days than that required at 14 days.
3. The mortar expansion decreased linearly with an
increase in the SiO2(eq) of total cementitious materials in the
mortar bar. Conversely, it increased proportionally with an
increase in the CaOeq and the CaOeq/SiO2(eq) of total binding
materials in the mixture.
4. The proposed analytical models were able to predict the
optimum dosage of Class F fly ash in suppressing the excess
mortar expansion of the six studied reactive aggregates
below the expansion limits at the test durations of 14, 28, and
56 days. A good agreement existed between the minimum
required Class F fly ash content evaluated by the experimental procedures and that predicted by the proposed empirical models of using the SiO2(eq), CaOeq, and CaOeq/SiO2(eq)
of total cementitious materials in the mortar bars.
ACI Materials Journal/January-February 2016
Mohammad S. Islam is a Postdoctoral Research Associate in the Department of Civil and Environmental Engineering and Construction at the
University of Nevada, Las Vegas, Las Vegas, NV.
Nader Ghafoori is a Professor in the Department of Civil and Environmental
Engineering and Construction at the University of Nevada, Las Vegas.
ACKNOWLEDGMENTS
REFERENCES
23
ASTM C1260, 2007, Standard Test Method for Potential Alkali Reactivity of Aggregates (Mortar-Bar Method), ASTM International, West
Conshohocken, PA, 5 pp.
ASTM C1567, 2007, Standard Test Method for Determining the Potential Alkali-Silica Reactivity of Combinations of Cementitious Materials and
Aggregate (Accelerated Mortar-Bar Method), ASTM International, West
Conshohocken, PA, 5 pp.
ASTM C305, 2014, Standard Practice for Mechanical Mixing of
Hydraulic Cement Pastes and Mortars of Plastic Consistency, ASTM International, West Conshohocken, PA, 3 pp.
Bach, F.; Thorsen, T. S.; and Nielsen, M. P., 1993, Load-Carrying
Capacity of Structural Members Subjected to Alkali-Silica Reactions,
Construction and Building Materials, V. 7, No. 2, pp. 109-115. doi:
10.1016/0950-0618(93)90040-J
Ballard, Z. J.; Caires, W. S.; and Peters, S. R., 2008, Alternate Mitigation Materials for Alkali-Silica Reaction (ASR) in Concrete, Report No.
CDOT-2008-10, DTD Applied Research and Innovation Branch, Colorado
Department of Transportation, Denver, CO, 72 pp.
Brub, M. A., and Fournier, B., 1993, Canadian Experience with
Testing for Alkali-Aggregate Reactivity in Concrete, Cement and Concrete
Composites, V. 15, No. 1-2, pp. 27-47. doi: 10.1016/0958-9465(93)90037-A
Bleszynski, R. F., and Thomas, M. D. A., 1998, Microstructural Studies
of Alkali-Silica Reaction in Fly Ash Concrete Immersed in Alkaline Solutions, Advanced Cement Based Materials, V. 7, No. 2, pp. 66-78. doi:
10.1016/S1065-7355(97)00030-8
Broekmans, M. A. T. M., 1999, Classification of the Alkali-Silica Reaction in Geochemical Terms of Silica Dissolution, Proceedings of the 7th
Euroseminar on Microscopy Applied to Building Materials, H. S. Pietersen,
J. A. Larbi, and H. H. A. Janssen, eds., Delft University of Technology,
Delft, the Netherlands, pp. 155-170.
Folliard, K. J.; Ideker, J.; Thomas, M. D. A.; and Fournier, B., 2004,
Assessing Aggregate Reactivity Using the Accelerated Concrete Prism
Test, Proceedings of the Seventh CANMET/ACI International Conference
on Recent Advances in Concrete Technology, SP-222, V. M. Malhotra, ed.,
American Concrete Institute, Farmington Hills, MI, pp. 269-283.
Hobbs, W. D., 1988, Alkali-Silica Reaction in Concrete, Thomas Telford,
London, UK, 183 pp.
Hooton, R. D., 1991, New Aggregate Alkali-Reactivity Test Methods,
Pep. MAT 91-14, Ministry of Transportation of Ontario, Research and
Development Branch, Toronto, ON, Canada, 83 pp.
Hooton, R. D., 1995, Test Procedures for ASR, Proceedings of the
Third Annual ICAR Symposium, Concrete, Bases, and Fines, Center for
Aggregates Research (ICAR), Austin, TX, 9 pp.
Hooton, R. D., and Rogers, C. A., 1993, Development of the
NBRI Rapid Mortar Bar Test Leading to its Use in North America,
Construction and Building Materials, V. 7, No. 3, pp. 145-148. doi:
10.1016/0950-0618(93)90051-D
Hudec, P., and Banahene, N., 1993, Chemical Treatment and Additives
for Controlling Alkali Reactivity, Cement and Concrete Composites, V. 15,
No. 1-2, pp. 21-26. doi: 10.1016/0958-9465(93)90036-9
Islam, M. S., 2010, Performance of Nevadas Aggregate on AlkaliAggregate Reactivity of Portland Cement Concrete, PhD dissertation,
Department of Civil and Environmental Engineering, University of Nevada,
Las Vegas, Las Vegas, NV, 362 pp.
Islam, M. S., and Akhtar, S., 2013, A Critical Assessment to the Performance of Alkali-Silica Reaction (ASR) in Concrete, Canadian Chemical
Transactions, V. 1, No. 4, pp. 253-266.
Jasso, A. J., 2012, Characterization of Fly Ash for Evaluating the Alkali-Silica Reaction Resistance of Concrete, masters thesis, The University
of Texas at Austin, Austin, TX, 115 pp.
Jin, W., 1998, Alkali-Silica Reaction in Concrete with Glass AggregateA Chemo-Physico-Mechanical Approach, PhD dissertation,
Columbia University, New York, NY, 154 pp.
Johnston, D.; Stokes, D.; and Surdahl, R., 2000, A Kinetic-Based
Method for Interpreting ASTM C 1260, Cement, Concrete and Aggregates, V. 22, No. 2, pp. 142-149. doi: 10.1520/CCA10474J
Johnston, D. P.; Stokes, D. B.; Fournier, B.; and Surdahl, R. W., 2004,
Kinetic Characteristics of ASTM C1260 Testing and ASR-Induced
Concrete Damage, Proceedings of the 12th International Conference on
Alkali-Aggregate Reaction in Concrete, Beijing, China, pp. 338-346.
Kerenidis, K., 2007, Mitigating Alkali-Silica Reaction in Concrete with
Supplementary Cementing Materials when Used in Conjunction with Portland Cements Having Alkali Contents in Excess of 1.0%, masters thesis,
University of Toronto, Toronto, ON, Canada, 233 pp.
Lger, P.; Cote, P.; and Tinawi, R., 1996, Finite Element Analysis of
Concrete Swelling Due to Alkali-Aggregate Reactions in Dams, Computers
& Structures, V. 60, No. 4, pp. 601-611. doi: 10.1016/0045-7949(95)00440-8
Leming, M. L.; Mitchell, J. F.; Johnson, J. K.; and Ahmad, S. H., 1996,
Investigation of Alkali-Silica Reactivity in North Carolina Highway Struc-
24
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