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Kim 2015
Kim 2015
h i g h l i g h t s
a r t i c l e i n f o a b s t r a c t
Article history: This research paper have evaluated the performance of durability of fibre-reinforced concrete through
Received 22 November 2014 various test methods exposed to pH 4.5 solutions for 27 months with uncracked and precracked beams.
Received in revised form 7 June 2015 The structural fibres used in this study were hooked end steel, polypropylene (PP) and polyvinyl alcohol
Accepted 8 June 2015
(PVA) fibres and the strong acid solutions were simulated with acetic acid at the laboratory. The evalu-
Available online 3 July 2015
ation methods for durability performance subsequent to conditioning included ultrasonic pulse velocity
(UPV), carbonation, residual strength and toughness. The additional tests such as absorption, permeabil-
Keywords:
ity and diffusion for transport properties of harmful materials were performed. The experimental results
Fibre
Erosion
showed significant reductions in both residual strength and toughness were found against low pH solu-
Transport property tions, as well as the analysis of ultra-pulse velocity (UPV) and carbonation for all fibre mixtures.
Residual strength Consequently, in case of steel fibre-reinforced concrete indicating good resistance to the movement of
Toughness harmful materials into concrete have excellent durability performance and then PVA, PP fibres in
sequence.
Ó 2015 Elsevier Ltd. All rights reserved.
http://dx.doi.org/10.1016/j.conbuildmat.2015.06.023
0950-0618/Ó 2015 Elsevier Ltd. All rights reserved.
B. Kim et al. / Construction and Building Materials 93 (2015) 720–728 721
to that of ettringite (hydration product). It causes the change of minute again. Then the remaining cement and 50% water as well as the high perfor-
mance water-reducing agent were added and mixed for two minutes. The fibres
microstructure by formation of salt crystalloid by physical reaction
were added lastly. After the mixing, the soft concrete was deposited in the
of sulfate ion and chemical reaction of sulfate ion with hydration 200 mm 400 mm 600 mm wooden mold for even diffusion of the fibres. To fab-
product [5]. Third, it is the performance degradation by chemical ricate the test sample for the beam experiment, the concrete was deposited into the
erosion of the structure exposed to the acid rain, wastewater treat- 100 mm 510 mm 360 mm steel mold and initially cured indoor at 23 ± 2 °C
ment plant, and hot spring. Ca(OH)2, which is the hydration pro- temperature and 50 ± 2% relative humidity for 24 h. Then the mold was removed
and the concrete was cured at a damp curing room with 100% relative humidity
duct that takes up to 20–30% of the cement pool solid volume, is
for 28 days. The cylindrical test sample with 10 mm diameter and 20 mm height
alkalic and thus vulnerable to the acid rain. Moreover, the hydrau- to measure the compressive strength was fabricated through coring on the 15th
lic compounds C–A–H and C–S–H also react with acid and are day of damp curing while the test sample for bending stiffness was fabricated by
decomposed. The hydration ion will accelerate the leaching of cal- cutting the sample into 100 mm 100 mm 360 mm after damp curing was
completed.
cium hydroxide (Ca(OH)2 + 2H+ ? Ca2+ + 2H2O). If the ion is highly
concentrated, C–S–H may also be attacked, forming silica gel
(3CaO2SiO23H2O + 6H+ ? 3Ca2+ + 2(SiO2nH2O) + 6H2O) [5]. The
type of acids eroding the concrete includes the inorganic acids (sul- 3. Experiment
furic acid, hydrochloric acid and acetic acid) and organic acids (lac-
tic acid and citric acid). Most concrete structures are eroded by 3.1. Workability test
these acids.
Various types of fibres have been used to improve the perfor- When the fibres are added to the concrete, the flow ability is
mance of concrete structures. They are added to the concrete to degraded because of increased stiffening during mixing. The work-
enhance the brittle property by improving the control of cracking, ability can be increased by adding the conventional or high perfor-
spalling, freeze–thawing, bending, etc. caused by drying shrinkage mance water-reducing agent or changing the mix design. However,
and eventually to improve the durability of the concrete. Although the slump test used for conventional concrete will not accurately
there have been many studies of evaluating the durability perfor- measure the workability of fibre reinforced concrete. That is
mance worldwide, most them focused on exposure to salt attack because the loss of slump value and the loss of workability do
[6]. not match when the concrete is reinforced with fibre [3]. This
This study evaluated the durability performance through the experiment observed the effect of flow ability change of each fibre
experimental observation of erosion resistance by fibre reinforce- with the slump test, which is the general workability measurement
ment in cement pool by exposing the fibre reinforced concrete to method, and the inverted slump cone test and Vebe test, which are
the acetic acid among the environmental factors exposed to chem- the plasticity property measurement method and then studied the
ical erosion. For the experiment, steel fibre, PP (polypropylene) correlation with the slump test.
fibre, and PVA (polyvinyl alcohol) fibre, which are widely used in Fig. 2 shows a picture of an inverted slump cone test. To mea-
construction sites worldwide, were selected [7–9]. The several sure the workability of fibre reinforced concrete, the concrete
kinds of methods were used to evaluate durability performance was fabricated according to the procedure specified in ASTM C
of steel and synthetic fibres, which include fresh properties as well 995 [10] and tested at the lab. A slump cone was fastened to a woo-
as hardened properties of FRC. The fresh properties were evaluated den frame upside down and placed at the top of a bucket so that
soon after fibres were added by measuring flow ability with there was around 10 cm gap between the bottom surface of the
inverted slump cone and Vebe time tests. Hardened property’s bucket and inverted slump cone. The inverted slump cone was
change of FRC were evaluated by performing flexural tests (resid- filled with the concrete in three times. Then the timer was pressed
ual strength and toughness after initiating concrete crack). as soon as the bottom plate was vibrated, and the time it took until
Additionally, to understand the effect of fibres for the movement the inverted slump cone was fully drained of concrete to evaluate
of harmful materials under environmental conditioning, transport the flow ability and consistency of the fibre reinforced concrete.
properties were measured with absorption, permeability and diffu- Because of the fibre used in the experiment, the workability and
sion tests. Finally, UPV and carbonation tests were used to evaluate flow ability of the concrete degraded significantly, and the fibre
the damage degree of FRC exposed to environmental conditioning. reinforced concrete did not flow naturally as the bottom hole of
the slump cone was plugged by the fibre reinforced concrete.
2. Experiment plan Fig. 3 shows a picture of a Vebe test. The purpose of Vebe test is
to measure the consistency of the very dry concrete and specified
2.1. Materials for experiment in ASTM C 1170 [11]. A slump cone was erected on a vibrating table
plate and filled with the concrete in three time. Then the slump
This study used the Class 2 moderate heat Portland cement, river sand with 2.65
specific gravity and 2.39 fineness modulus as fine aggregates, and crushed aggre- cone was removed, the top plastic plate was brought in contact
gates with 9.5 mm maximum size and 2.28 specific gravity as coarse aggregates. on top of the concrete surface, and a timer was pressed as soon
The steel fibre used in the experiment was the collated hooked type with 30 mm as it began vibrating. The time it took until the slump was com-
length, 560 lm diameter and 55 aspect ratio manufactured by a company B in pletely collapsed was measured.
another country, which is the most widely used steel fibre in the steel fibre rein-
forced concrete. The steel fibre is vulnerable to alkalic and acid. The PP fibre was
the single fibre type with 30 mm length, 660 lm diameter and 45 aspect ratio man-
ufactured by a company K in another country. It is relative vulnerable to strong acid. 3.2. Compressive strength test
The PP and PVA fibres were developed by manufacturers to supplement and replace
the weakness of the structural steel fibre. Fig. 1 shows the type and shape of the
To evaluate the impact of contents and reinforcement effects in
fibres. Table 1 shows the physical properties of the steel fibre, PP fibre and PVA fibre
used in this experiment. the cement pool of steel fibre, PP fibre and PVA fibre on concrete
compressive strength, the compressive strength experiment was
2.2. Mix design and curing conducted in accordance with ASTM C 39 [12]. The cylindrical sam-
ple of 100 mm diameter and 200 mm height was fabricated
Table 2 shows the mix design of each fibre. Each of 4.6 kg/m3 PP fibre (M2 and through the coring during the curing process of the fibres evenly
M6), 9.7 kg/m3 PVA fibre (M3 and M7), and 70.8 kg/m3 was mixed steel fibre (M4
and M8) into two types of water-cement mix. For mixing the concrete, the fine
diffused in the concrete for the experiment. After water curing
aggregates and coarse aggregates were poured into a forced pan type mixer first for 28 days, universal testing machine (UTM) with 2000 kN capac-
and dry mixed for one minute. Then 50% water was added and mixed for one ity was used.
722 B. Kim et al. / Construction and Building Materials 93 (2015) 720–728
Table 1 exposed to the atmosphere, the distance water moved per time
Physical property of fibre. was measured. The experiment related to the diffusional behavior
Property Steel PP PVA of chorine ion was conducted according to ASTM C 1556 [15] using
Density 7.85 0.9 1.3
three test samples. The samples were cut into 100 mm 100 mm
Diameter (lm) 560 430 660 pieces, and the surface except the exposed surface were coated
Length (mm) 30 39 30 with epoxy and immersed in the 16.5% sodium chloride solution
Aspect ratio (l/d) 55 90 45 indoor for a year. The solution was replaced every 5 weeks. After
Tensile strength (MPa) 1100 620 800
one year of immersion, the samples were cut in parallel to the
Elastic modulus (GPa) 200 9.5 29
Acid resistance Low High Low exposed surface then grinded into fine particles. The amount of
chlorine ion contained in a unit volume was measured. The diffu-
sion coefficient of chlorine ion was measured using Fick’s second
3.3. Harmful material transfer property test law of diffusion.
Table 2
Mix Proportions.
3.6. Carbonation
The depth of each test sample after erosion began was observed
by checking the color change by cutting the beam after the beam
experiment, cleaning its surface and then spraying the phenolph-
thalein solution on the destroyed area. Since the phenolphthalein
solution turns into violet color at pH of 9.0–9.5, the part of lower
acidity because of carbonation has no color change. The degree of
carbonation was devaluated by measuring with a micrometer the
depth of the part whose surface color did not change.
5. Experiment results
Table 3
Workability test results.
Mix type Fiber type Slump (mm) I.S.C.T* (s) Vebe time (s)
M1 – 146 15 2
M2 PP 25 99 7
M3 PVA 38 85 6
M4 Steel 19 87 9
M5 – 83 32 4
M6 PP 45 78 6
M7 PVA 70 67 4
M8 Steel 45 59 5
⁄
Inverted slump cone time.
Table 4
Compressive strength results.
Table 5
Transport properties of harmful materials.
that order when the beam test sample is exposed to the erosive
environment.
Fig. 12. Residual strength reduction percent between limewater and pH 4.5
Fig. 11. Test results for uncracked beam (toughness). solutions.
shows the change of toughness according to the fibre type and mix same environment, the difference of ultrasonic pulse speed by
ratio. It indicates that erosion under the strong acid caused the the crack was not large. However, the test sample exposed to the
lower toughness than the reference test sample and that the steel acidic solution showed 20–25% lower speed than the reference test
fibre had the most outstanding toughness regardless of the sample. That is attributed to the deterioration of durability due to
exposed environment. the decrease of dynamic property of the beam test sample by ero-
sion of the surface [19]. PP and PVA fibre reinforced test samples
generally had the low UPV while the steel fibre reinforced test
5.5. Ultrasonic pulse velocity sample had the high UPV. Because of the change of UPV, the
decrease of durability performance of the beam test sample
Fig. 14 shows the result of ultrasonic pulse measured before the showed the similar trend as the change of residual strength and
beam sample was destroyed. For the test samples exposed to the toughness.
Table 6
Residual strength results.
Mix type Exposure conditioning Residual load (kN) Residual strength (MPa) Specimen condition
0.5 mm 0.77 mm 1 mm 0.13 mm
M1 Limewater – – – – – Precracked beam
pH 4.5 – – – – –
M2 Limewater 7.11 7.86 8.02 8.0 2.15
pH 4.5 2.75 3.04 3.22 3.32 0.90
M3 Limewater 10.01 10.46 8.72 6.17 2.50
pH 4.5 2.32 2.57 2.73 2.87 0.74
M4 Limewater 20.84 19.22 17.90 16.48 5.31
pH 4.5 8.84 8.56 8.29 8.04 2.36
M5 Limewater – – – – –
pH 4.5 – – – – –
M6 Limewater 5.85 6.20 8.94 8.86 2.39
pH 4.5 3.50 3.92 4.20 4.35 1.13
M7 Limewater 7.98 8.68 8.17 6.44 2.22
pH 4.5 4.94 5.50 5.88 5.96 1.57
M8 Limewater 23.29 21.64 20.32 19.25 5.84
pH 4.5 9.56 9.31 8.98 8.43 2.58
M1 Limewater – – – – – Uncracked beam
pH 4.5 – – – – –
M2 Limewater 5.09 5.38 5.56 5.63 1.72
pH 4.5 3.36 3.56 3.24 3.82 0.89
M3 Limewater 8.21 9.16 9.33 8.71 2.73
pH 4.5 2.65 2.93 3.05 3.09 0.81
M4 Limewater 18.38 17.32 15.80 14.33 4.65
pH 4.5 9.45 9.40 9.30 8.79 2.63
M5 Limewater – – – – –
pH 4.5 – – – – –
M6 Limewater 5.85 6.20 6.35 6.34 1.73
pH 4.5 3.69 3.96 4.15 4.30 1.15
M7 Limewater 6.03 6.49 6.68 6.03 1.84
pH 4.5 3.87 430 4.67 4.98 1.28
M8 Limewater 21.70 20.72 19.16 18.21 3.68
pH 4.5 14.09 14.08 13.84 13.47 2.50
B. Kim et al. / Construction and Building Materials 93 (2015) 720–728 727
and corner cross section of the test sample. The visual inspection of
the cutting plane indicates the serious corrosion at the edge of the
surface. The phenolphthalein solution was sprayed on the surface,
and the color change was observed. That the carbonation depth
was measured using a micrometer. Fig. 16 shows the carbonation
depth according to mixing and cracks on the test sample. There
was no carbonation on the reference test sample, but the car-
bonization was observed on the test sample exposed to the acidic
solution. There was no large difference in carbonation depth
according to the crack. In the test samples without cracks, the PP
fibre showed relatively faster carbonation in the high strength
mixing while the steel fibre showed slower carbonation. That is
consistent to the expected result of harmful material transport
characteristics.
6. Conclusions