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Ultra-High Strength Concrete Mixtures Using Local Materials

Srinivas Allena1 and Craig M. Newtson2


1
New Mexico State University, Civil Engineering Department, P.O. Box 30001, MSC
3CE, Las Cruces, NM 88003-8001; PH: (575) 571-9490; FAX: (575) 646-6049; email:
srinivas@nmsu.edu
2
New Mexico State University, Civil Engineering Department, P.O. Box 30001, MSC
3CE, Las Cruces, NM 88003-8001; PH: (575) 646-3034; FAX: (575) 646-6049; email:
newtson@nmsu.edu

Abstract

This paper presents the development of ultra high strength concrete (UHSC) using
local materials. UHSC mixture proportions were developed using local materials so that
UHSC may be made more affordable to a wider variety of applications. Specifically,
local sand with a top size of 0.0236 in. (600 μm), and locally available Type I/II cement
and silica fume were used in this research. Each of these material selections is seen as an
improvement in sustainability for UHSC. Two mixtures (one with and one without fibers)
were recommended as the UHSC mixtures. The greatest compressive strengths obtained
in this study were 24,010 psi (165.6 MPa) for UHSC with steel fibers and 23,480 psi
(161.9 MPa) for UHSC without fibers. The compressive and flexural strengths obtained
from the UHSC mixtures developed in this work are comparable to UHSC strengths
presented in the literature. Producing this innovative material with local materials reduces
the cost of the material, improves sustainability, and produces mechanical performance
similar to prepackaged, commercially available products.

Introduction

In the past several years, improvements have been occurring in concrete


technology. Sustainable use of supplementary materials and revolutionary developments
in superplasticizing admixtures have facilitated improvements in the mechanical
properties and durability of concrete. For example, researchers are using silica fume and
high range water reducing admixtures to produce high density concrete. In addition to the
use of mineral and chemical admixtures, applying pre-setting pressure and using post-
setting heat treatment can also be used to produce dense microstructure. Other techniques
intended to increase concrete density include using numerical packing models (de Lerrard
and Sedron 1994). Numerical packing models predict the packing density of a particle
mixture. Packing density is the volume of solids in a unit volume (Ferraris and de Larrard
1998). Using these methods, compressive strengths greater than 29,000 psi (200 MPa)
have been achieved (Richard and Cheyrezy 1995).
In addition to high strength, the concrete should exhibit greater durability
characteristics. This means that the concrete should be high strength and high
performance. One of the materials developed in recent years is ultra high strength
concrete (UHSC) also known as reactive powder concrete (RPC). This material possesses
a compressive strength greater than 21,750 psi (150 MPa). The concept of RPC was first

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developed by Richard and Cheyrezy (1994) and was first produced in the early 1990s by
researchers at Bouygues‫ ׳‬laboratory in France (Dili and Santhanam 2004). This new
material is usually produced with cement, fine quartz sand, silica fume, steel fibers and
high range water reducing admixture (HRWRA). Very low water-to-cementitious
materials ratios are used to produce this kind of concrete. In a more accurate sense,
UHSC is not concrete because it contains no coarse aggregate (Collepardi et al. 2007).
The steel fibers provide ductility to UHSC. This material differs from conventional
concrete not only in terms of strength, but also in terms of durability. UHSC is more
durable because the low water-to-cementitious materials ratio results in very low porosity
(Roux et al. 1996). The possibility of achieving high strength, durability, and improved
ductility with the use of ultra high strength concrete encourages researchers and engineers
to use this modern material in many practical applications like nuclear waste containment
structures, high rise structures, long span bridges, and walkways.
In the present research, an attempt has been made to develop UHSC mixtures with
locally available materials. The materials used in this work included Type I/II portland
cement, silica fume, fine sand (passing ASTM No. 30 sieve), 0.5 in. (13 mm) long steel
fibers, and HRWRA. Mixtures with and without steel fibers were prepared and tested to
study the effects of steel fibers on compressive strength and tensile strength. Factors such
as age and curing regimen were also investigated.

Background

UHSC is composed of cement, fine sand, quartz powder, micro silica, steel fibers
and HRWRA. When used in optimum dosages, the HRWRA reduces the water- to-
cementitious materials ratio while improving the workability of concrete. The addition of
micro silica enhances the mechanical properties of the paste by filling voids, enhancing
rheology, and producing secondary hydrates. The quartz powder is useful for its
reactivity during heat treatment (Dili and Santhanam 2004). The constituents of the
mixture and proportions (by fraction of cement mass) proposed by various investigators
(Richard and Cheyrezy 1995, Shaheen and Shrive 2006, and Matte and Moranville 1999)
are presented in Table 1.
Roux et al. (1996) demonstrated that the mechanical properties of RPC are
obtained by lowering the water-to-cementitious materials ratio, using HRWRA’s, and
including silica fume. The lower water-to-cementitious materials ratio reduces the
porosity of the cement paste and improves durability. Richard and Cheyrezy (1995)
recommended the following principles to develop UHSC:

• Removal of coarse aggregate to enhance homogeneity of the concrete.


• Use of silica fume for pozzolanic reaction.
• Optimization of the granular mixture for enhancement of compacted density.
• Application of presetting pressure for better compaction.
• Post-setting heat treatment to enhance the mechanical properties of the
microstructure.
• Addition of steel fibers to achieve ductility.

2010 Concrete Sustainability Conference 2 © National Ready Mixed Concrete Association


Sustainability

Materials used in UHSC such as quartz dust and steel aggregate are often shipped
long distances, internationally in many cases, increasing the cost of the material.
Additionally, strict requirements on the chemistry of the cement and silica fume increase
the cost of commercially available, prepackaged UHSC products such as Ductal.
Expensive materials such as ground quartz and fibers that are not available locally are
used in the production of Ductal, resulting in increased cost of the final product.
Therefore, the present work focused on developing UHSC mixture proportions using
local materials so that UHSC may be made more affordable to a wider variety of
applications. Specifically, local sand with a top size of 0.0236 in. (600 μm), and locally
available Type I/II cement and silica fume were used in this research. Each of these
material selections is seen as an improvement in sustainability for UHSC. Reduced
member sizes are also possible with UHSC, which reduces the volume of concrete used
to produce a given structural element.

Experimental Program

Materials. Type I/II portland cement, silica fume, and fine local sand (0.00295-0.0236 in
[75-600 μm]) from Las Cruces, New Mexico were used. Table 2 shows the grain size
distribution for the fine sand. The chemical compositions of the Type I/II portland cement
and silica fume are provided in Table 3. Steel fibers that were 0.5 in. (13 mm) long were
used to provide ductility. To achieve the desired workability, a commercially available
polycarboxylate-based HRWRA (Glenium 3030 NS from BASF Chemicals) was used.

Concrete Mixtures. Table 4 shows the mixture proportions, the water-to-cement ratio
and the water-to-cementitious materials ratio (including silica fume) for a group of 7
mixtures investigated during the development of the UHSC. These mixtures were divided
into five categories. Several other mixture proportions were also evaluated. However,
only these mixtures are presented for the sake of brevity. The mixtures were categorized
as follows:

A : The mixture in this category used Type I/II portland cement and HRWRA.
The aggregates for this mixture were thoroughly washed and dried prior to use.
Steel fibers were used to fill 1.5% of the volume. However, no silica fume was
used in this mixture.

B : The mixtures in this category also used Type I/II portland cement and
HRWRA and the aggregates were thoroughly washed and dried prior to use.
Silica fume and steel fibers were both used in these mixtures.

C and D: The mixtures in these categories used Type I/II portland cement and
HRWRA. The aggregates were thoroughly washed and dried prior to use. Silica
fume was used in these mixtures. However, steel fibers were not used in these
mixtures. The mixture in category D had lower water-to-cement and water-to-
cementitious materials ratios than the mixtures in category C.

2010 Concrete Sustainability Conference 3 © National Ready Mixed Concrete Association


E: The mixture in this category used Type I/II portland cement and HRWRA and
the aggregates were thoroughly washed and dried prior to use. Both silica fume
and steel fibers were used in this mixture. The mixture in this series had a water-
to-cement ratio and a water-to-cementitious materials ratio that was lower than
those used for the series B mixtures.

Mixtures within each category were assigned a name. Mixture names were four
digit symbols where the first letter referenced the category for the mixture, the second
letter referred to the source of the aggregate, and the last two numbers referred to the
percentage increase in water and cementitious materials content over the base mixture.
For example, mixture BL20 was a mixture from category B that used aggregates from
Las Cruces, New Mexico and had 20% more water, cement, and silica fume than the base
mixture (BL00).

Specimen Preparation. Sand used in this study was passed through a No. 30 sieve to
obtain the desired particle sizes. The aggregates were then thoroughly washed over a No.
200 sieve. After washing, the sand was oven dried at 110°F (44°C) to achieve 0%
moisture content.
The constituents of each mixture were mixed for 15 to 20 minutes using a
laboratory pan mixture. The dry constituents were mixed for 2 minutes and then 75% of
the water was added. After thorough mixing, the HRWRA was added and the remaining
25% of the water was added to the mixture. Steel fibers were added at the end. This
process of mixing seemed to improve the action of the HRWRA.
Compressive strength specimens included 2 in. (50 mm) cubes and 4 by 8 in.
(100 by 200 mm) cylinders. To avoid problems with end preparation of cylinder
specimens, only 2 in. (50 mm) cubes were used as compressive strength specimens for
mixture categories C, D, and E. Modulus of rupture testing was conducted on 3x4x16 in.
(75x100x400 mm) prisms. All specimens were consolidated using a high frequency
vibrating table.

Curing Regimens. Three curing regimens were investigated. For the first regimen,
concrete specimens were cured at room temperature, 65°F (20°C), for the first 24 hours.
After demolding, the specimens were moist cured at a temperature of 73.4°F (23°C) and
a relative humidity of 100% until the day of testing and this curing regimen was
designated as MC.
In the second curing regimen, concrete specimens were cured at room
temperature, 65°F (20°C), for the first 24 hours. After demolding, the specimens were
heat cured in a water bath at 122°F (50°C) until the time of testing. This curing regimen
was designated as WB.
For the third curing regimen, concrete specimens were cured at room temperature,
65°F (20°C), for the first 24 hours. After demolding, the specimens were heat cured in a
water bath at 122°F (50°C). Then, the specimens were removed from the water bath and
dry cured at 392°F (200°C) for two days prior to testing. This curing regimen was
designated as OV.

2010 Concrete Sustainability Conference 4 © National Ready Mixed Concrete Association


Compression Testing. Compression tests were conducted on 2 in. (50 mm) cubes and 4
by 8 in. (100 by 200 mm) cylinders to evaluate the compressive strength of UHSC. After
the specified curing period, cylindrical specimens were tested according to ASTM C 39
and cube specimens were tested according to BS 1881-116.

Modulus of Rupture Testing. Prismatic specimens that were 3x4x16 in. (75x100x400
mm) were tested to evaluate modulus of rupture. Modulus of rupture was determined
using a third point loading test on prism specimens according to ASTM C 78. Specimens
were rotated 90 degrees from the orientation in which they were cast to measure the
flexural strength. Consequently, the 4 in. (100 mm) dimension was aligned with the
direction of loading.

Compressive Strength Results and Discussion

Average compressive strengths of specimens produced from each mixture


category are presented in Table 5. To investigate the repeatability of the compressive
strengths of these mixtures, testing was conducted on three specimens cast from each of
four different batches. Compressive strengths were measured at 7, 14, and 28 days. The
aggregates were thoroughly washed and dried prior to use to remove any dust. A better
coating of cement paste over the sand particles was achieved by removing the dust,
resulting in increased compressive strengths.

Category A. In the process of developing UHSC, mixture AL00 was produced as the
first trial mixture. AL00 was produced with a water-to-cement ratio of 0.28 and no silica
fume was used in this mixture. Compression tests were conducted on 4 by 8 in. (100 by
200 mm) cylinders after 7 days of moist curing. Mixture AL00 produced a compressive
strength of 6940 psi (47.86 MPa). This compressive strength was considered low in
comparison to the usual compressive strength range for UHSC. The low compressive
strength of mixture AL00 was initially attributed to the absence of silica fume. Therefore,
the subsequent mixtures (categories B, C, D, and E) in the research were produced using
silica fume.

Category B. Mixtures in category B were produced by modifying the mixture


proportions of AL00. To produce mixture BL00, silica fume was used to replace 24.5%
of the cement that was used in AL00. BL00 contained 8.6% less sand and 36.84% less
HRWRA than AL00. The steel fiber content was maintained at 1.5%. The water-to-
cementitious materials ratio of BL00 was equal to the water-to-cement ratio of AL00.
Cylindrical specimens produced from mixture BL00 were moist cured until 7 days and
then tested for compressive strength. The compressive strength of specimens produced
from BL00 was 6880 psi (47.45 MPa) which is marginally lower (0.86%) than the
compressive strength from mixture AL00.
The compressive strengths of AL00 and BL00 were lower than expected.
However, it was felt that increasing the volume of the paste may improve the
compressive strength. Consequently, the quantities of cement, silica fume, and water
were increased by 20% over the base mixture (BL00) to produce mixture BL20. Since the
percent increase was the same for cement, silica fume, and water, the water-to-

2010 Concrete Sustainability Conference 5 © National Ready Mixed Concrete Association


cementitious materials ratio did not change. The percent volume of paste was 71.3% for
BL20 which was 11.9% more than the paste volume for BL00 (59.4%). The specimens (4
by 8 in. [100 by 200 mm] cylinders) produced from mixture BL20 were moist cured and
tested for compressive strength at 7, 14, and 28 days. The compressive strengths at 7, 14,
and 28 days were 7080 psi (48.83 MPa), 8090 psi (55.79 MPa), and 9210 psi (63.52
MPa), respectively.
The compressive strengths obtained from the mixture BL20 were still too low for
UHSC. In another attempt to increase compressive strength, it was decided to accelerate
the hydration reaction by employing post setting heat treatment. To accomplish this,
specimens produced from BL20 were cured according to curing regimen WB. The
elevated curing temperature (122°F [50°C]) resulted in increases of 19%, 6.7%, and 4.8%
in compressive strengths measured at 7, 14, and 28 days, respectively.

Category C. For the next step in trying to improve the compressive strength, the water-
to-cementitious materials ratio was reduced to 0.22 (from 0.28 for BL00) to produce
mixture CL00.The reduced water-to-cement ratio was produced by increasing the cement
content by 25.31% and decreasing the water content by 7% (compared to BL00). No steel
fibers were used in mixture CL00, and the sand content in CL00 was reduced by 5.5%
compared to BL00.
At this stage, it was decided to use cube specimens for compression testing to
avoid problems with the end preparation of cylinder specimens. Compressive strengths
for all remaining mixtures were measured using 2 in. (50 mm) cube specimens. The size
of the cubes was selected such that the cube dimension was at least four times the size of
the largest particle used in the concrete (0.5 in. [13 mm] steel fibers). CL00 specimens
were cured according to curing regimen WB and tested at 7, 14, and 28 days. The
compressive strengths measured at 7, 14, and 28 days were 14,080 psi (97.10 MPa),
14,250 psi (98.28 MPa), and 16,250 psi (112.06 MPa), respectively.
To produce mixture CL20, CL00 was further modified by increasing the paste
volume. The percent volume of paste was 62.85% for CL00 and 75.44% for CL20. Cube
specimens produced from mixture CL20 were also cured according to curing regimen
WB and tested for compressive strength at 7, 14, and 28 days. The compressive strengths
at 7, 14, and 28 days were 13,560 psi (93.52 MPa), 14,360 psi (99.03 MPa), and 15,200
psi (63.52 MPa), respectively.
The next step in attempting to increase compressive strength was to try to
accelerate the pozzolanic reaction of the silica fume. To accelerate the pozzalonic
reaction of the silica fume, concrete specimens produced from CL00 were cured
according to curing regimen OV. A similar curing regimen was adopted by Reda et al.
(1999). Curing of concrete specimens at autoclave temperatures between 392ºF and
572ºF (200ºC and 300ºC) has been shown to accelerate the pozzalonic reaction and help
in the formation of dense calcium silicate hydrate compounds (Shaheen and Shrive
2006). In this study, curing at 392ºF (200ºC) was achieved in an oven. There were
concerns that dry curing may artificially inflate the compressive strengths. However, no
adverse effects were observed in flexural strength testing. This seems to indicate that
strength gains caused by oven dry curing at 392ºF (200ºC) were primarily due to the
accelerated pozzolanic reaction, not drying. Compressive strengths of the specimens
produced from CL00 (OV) were greater than the compressive strengths of specimens

2010 Concrete Sustainability Conference 6 © National Ready Mixed Concrete Association


produced from CL00 (WB) by 2.13%, 15.8%, and 5.35% at 7, 14, and 28 days,
respectively.
Category D. The water-to-cementitious materials ratio of CL00 was reduced to 0.20 to
produce mixture DL00. To improve the workability of DL00, the HRWRA dosage was
increased from 5 gal/yd3 (24.70 l/m3) to 6 gal/yd3 (29.64 l/m3). Specimens produced
from mixture DL00 were cured according to curing regimens WB and OV. Compressive
strengths achieved with mixture DL00 (OV) were 20,010 psi (138.55 MPa), 22,210 psi
(153.17 MPa), and 23,480 psi (161.90 MPa) at 7, 14, and 28 days, respectively. These are
increases of 39.2%, 34.6%, and 37.2% from CL00 at 7, 14, and 28 days, respectively.
The greater compressive strengths are attributed to the reduced water-to-cementitious
materials ratio.

Category E. Mixture EL00 was produced by introducing steel fibers to the mixture
proportions from DL00. The volume of sand was reduced by the volume occupied by
steel fibers in mixture EL00. Specimens produced from EL00 were cured according to
curing regimen OV. The greatest compressive strengths among all the mixture categories
used in this investigation were achieved using mixture EL00. The compressive strengths
achieved at 7, 14, and 28 days were 21,180 psi (146.06 MPa), 23,420 psi (161. 52 MPa),
and 24,010 psi (165.60 MPa), respectively. The greater compressive strength of the fiber
reinforced UHSC mixture is consistent with results reported by Reda et al. (1999).
Mixtures DL00 (OV) and EL00 (OV) were identified as UHSC and will be considered
for further research.

Strength Gain Versus Time. Compressive strength gain with time was investigated by
considering the plain (CL00 and DL00) and fiber reinforced (EL00) concrete mixtures.
All of the specimens were cured according to curing regimen OV. The ratios of
compressive strength at 7 and 14 days with respect to 28 day strength (assuming
compressive strength at 28 days is 100%) of mixtures CL00, DL00, and EL00 are
presented graphically in Figure 1. For mixtures CL00 and DL00, compressive strengths at
7 days were 84.0 and 85.6 percent of 28-day compressive strength, respectively. This
percentage was 88.2 for mixture EL00. Compressive strengths for CL00 and DL00 at 14
days were 96.4 and 94.6 percent of 28-day compressive strength, respectively, whereas
this percentage was 97.5 for mixture EL00. This strength development is more rapid than
the strength development of normal strength concrete and is attributed to the high
cementitious content of the UHSC mixtures and post-setting heat treatment that increased
the rate of the hydration reaction.

Curing Regimens. Curing regimen significantly influenced the compressive strength of


UHSC. Specimens cured according to curing regimen OV exhibited the greatest
strengths. Compressive strengths of specimens from mixtures DL00 cured according to
curing regimen OV and tested at 7 days were 20.0% greater than compressive strengths
of specimens cured in a water bath. However, this increase in strength was only 7.22% at
28 days. The greater compressive strength exhibited by oven dried specimens is
attributed to acceleration of the hydration reaction when the specimens were kept in
water bath 122°F (50°C) and the formation of secondary calcium silicate hydrate (CSH)
from the pozzolanic reaction of silica fume when the specimens were kept in an oven at

2010 Concrete Sustainability Conference 7 © National Ready Mixed Concrete Association


392°F (200°C) for two days prior to testing. These observations are similar to those
reported by Shaheen and Shrive (2006).

Effects of Steel Fibers. The effects of steel fibers on compressive strength of UHSC
were investigated by considering mixtures DL00 (without fibers) and EL00 (with fibers).
The specimens from both of these mixtures were cured according to the OV curing
regimen. Figure 2 illustrates the influence of steel fibers on compressive strength of
UHSC mixtures. The average percentage increase in compressive strength due to the
presence of steel fibers was 5.43, 5.45, and 2.25 percent at 7, 14, and 28 days,
respectively.

Modulus of Rupture Results and Discussion

One concern with UHSC specimens cured at elevated temperatures was that drying of the
sample might artificially inflate the compressive strength of the sample and decrease the
flexural strength. However, it was also believed that steel fibers would improve the
ductility of the concrete and could also increase the flexural strength of the concrete. To
investigate these potential effects, modulus of rupture was measured on 3x4x16 in.
(75x100x400 mm) prismatic specimens.
Average flexural strengths from mixture categories A, B, D, and E, measured at 7
days, are presented in Table 6. It can be seen from Table 6 that the greatest flexural
strength was obtained with mixture EL00 (2655 psi [18.31 MPa]). This strength is
consistent with flexural strengths obtained by other investigators for UHSC produced
without dry curing. Again, this indicates that the dry curing at 392°F (200°C) served to
accelerate the pozzolanic reaction of the silica fume.
A significant effect of steel fibers on the flexural strength of UHSC was also
observed (Table 6). The flexural strength of the UHSC with fibers (EL00) was greater
than that of the plain mixture (DL00) by 68.3%. The flexural strengths of plain and fiber
reinforced UHSC mixtures and the percentage increase in flexural strength due to
addition of steel fibers were consistent with the literature (Collepardi et al. 2007 and Dili
and Santhanam 2004).

Conclusion

This paper summarizes several steps in the development of UHSC using local
materials. The conclusions drawn during the course of this work are:
1. UHSC was developed with materials locally available in Las Cruces, New
Mexico that produced a compressive strength of 24,010 psi (165.6 MPa) and a
flexural strength of 2655 psi (18.3 MPa).
2. The strength properties of UHSC produced with local materials were similar to
those provided by prepackaged, commercially available products such as Ductal.
3. Prolonging the mixing period increased the workability of the mixtures.
4. Specimens cured with oven drying attained greater strength than specimens that
were moist cured or cured in a 122°F (50°C) water bath. The greater compressive
strength exhibited by oven dried specimens was attributed to the acceleration of
the hydration reaction when the specimens were kept in a water bath 122°F

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(50°C) and the formation of secondary calcium silicate hydrate from the
pozzolanic reaction of silica fume when the specimens were kept in an oven at
392°F (200°C) for two days prior to the testing.
5. Compressive strength of fiber reinforced UHSC (EL00) was greater than the
compressive strength of plain UHSC (DL00) at all ages. The percentage increases
in compressive strength due to steel fibers at 7, 14, and 28 days were 5.43, 5.45,
and 2.25 percent, respectively.
6. The flexural strength of UHSC containing steel fibers was 68% greater than the
flexural strength of UHSC that did not contain fibers.

Recommendations for Future Work

1. To improve sustainability, fly ash should be considered for use as a partial


replacement for silica fume and cement.
2. Efforts should be made to reduce temperature of 392°F (200°C) that was used in
the present work for the OV curing regimen. This would reduce energy costs.
3. Polypropylene fibers should be used in place of steel fibers to reduce the shipping
costs.
4. Shrinkage should be characterized throughout the curing process.
5. Mechanical properties such as modulus of elasticity and split tensile strength of
UHSC should be investigated.
6. Durability issues such as delayed ettringite formation, alkali-silica reaction,
freeze-thaw durability, and corrosion resistance of UHSC should be investigated.

References

Collepardi, S., Coppola, L., Troli, R., and Collepardi, M. (2007). “Mechanical Properties
of Modified Reactive Powder Concrete.”
www.encosrl.it/enco%20srl%20ITA/servizi/pdf/high/12.pdf.
Dili, A. S., and Santhanam, M. (2004). “Investigations on Reactive Powder Concrete: A
Developing Ultra High Strength Technology.” The Indian Concrete Journal,
78 (4), 33-38.
de Lerrard, F., and Sedran, T. (1994). “Optimization of Ultra-High Performance
Concrete by the Use of a Packing Model.” Cement and Concrete Research, 24
(6), 997-1009.
Ferraris, C.F., and de Larrard, F. (1998). “Testing and Modeling of Fresh Concrete
Rheology.” Building and Fire Research Laboratory, No. NISTIR 6094,
National Institute of Standards and Technology, Gaithersburg, MD, 1-61.
Matte, V., and Moranville, M. (1999). “Durability of Reactive Powder Composites:
Influence of Silica Flume on the Leaching Properties of Very Low
Water/Binder Pastes.” Cement and Concrete Composites, 21, 1-9.
Reda, M.M., Shrive, N.G., and Gillott, J.E. (1999). “Microstructural Investigation of
Innovative UHPC.” Cement and Concrete Research, 29 (3), 323-329.
Richard, P., and Cheyrezy, M. (1995). “Composition of Reactive Powder Concrete.”
Cement and Concrete Research, 25 (7), 1501-1511.

2010 Concrete Sustainability Conference 9 © National Ready Mixed Concrete Association


Richard, P., and Cheyrezy, M. H. (1994). “Reactive Powder Concretes with High
Ductility and 200-800 MPa Compressive Strength.” in Mehta, P.K. (Ed.),
Concrete Technology: Past, Present and Future, Proceedings of the V.
Mohan Malhotra Symposium, ACI SP 144-24, 507-518. Detroit: Victoria
Wieczorek.
Roux, N., Andrade, C., and Sanjuan, M. A. (1996). “Experimental Study of Durability of
Reactive Powder Concretes.” Journal of Materials in Civil Engineering, 8 (1),
1-6.
Shaheen, E., and Shrive, N. J. (2006). “Optimization of Mechanical Properties and
Durability of Reactive Powder Concrete.” ACI Materials Journal, 103 (6),
444-451.

Table 1. Mixture proportions (by fraction of cement) of UHSC from literature


Matte and
Shaheen and Shrive
Richard and Cheyrezy (1995) Moranville
( 2006)
(1999)
Constituent Carbon
Steel fibers
Fibers
Plain (0.5 in. Plain Steel fibers
(0.118 in. [3
[13 mm] long)
mm] long)
Portland cement 1 1 1 1 1 1 1
Silica fume 0.25 0.23 0.25 0.23 0.23 0.23 0.325
Quartz Sand 1.1 1.1 1.1 1.1 1.1 0.5 1.43
Quartz powder - 0.39 - 0.39 - - 0.3
Crushed quartz - - - - 0.39 0.39 -
Superplasticizer 0.016 0.019 0.016 0.019 0.019 0.019 0.018
Steel fibers - - 0.175 0.175 - - 0.275
Carbon fibers - - - - - 0.125 -
Water 0.15 0.17 0.17 0.19 0.13 0.13 0.2
w/c 0.15 0.17 0.17 0.19 0.13 0.13 0.2
w/cm 0.12 0.138 0.136 0.154 0.11 0.11 0.15
Pre-setting pressure, 3.8 3.8
- - - - -
ksi (MPa) (26) (26)
Post-setting heat
68 194 68 194 212 212 194
treatment
(20) (90) (20) (90) (100) (100) (90)
temperature, ˚F (˚C)

2010 Concrete Sustainability Conference 10 © National Ready Mixed Concrete Association


Table 2. Grain size distribution of fine sand

Sieve size, in. Percentage


Sieve No.
(mm) passing
0.0236
30 100
(0.60)
0.0118
50 40.1
(0.30)
0.0059
100 0
(0.15)

Table 3. Chemical compositions of cement and silica fume

Compound Cement Silica fume


SiO2 20.3% 96.9%
Al2O3 4.60% 0.20%
Fe2O3 3.40% 0.20%
CaO 63.9% 0.30%
K2O NA 0.30%
Na2O 0.55% (Equiv.) 0.20%
MgO 1.91% 0.20%
SO3 2.86% 0.10%

Table 4. Mixture proportions of UHSC

Silica Fine Steel w/


Category Mixture Cement Water HRWRA w/c
fume sand fibers (c+sf)
lb/yd3 lb/yd3 lb/yd3 lb/yd3 lb/yd3 gal/yd3
(kg/m3) (kg/m3) (kg/m3) (kg/m3) (kg/m3) (l/m3)
1585 1558 321 444 4.75
A AL00 - 0.28 0.28
(940) (924) (190) (263) (23.50)
1197 388 1424 321 444 3.00
BL00 0.37 0.28
(710) (230) (844) (190) (263) (14.80)
B 1436 466 903 319 532 3.25
BL20 0.37 0.28
(852) (276) (535) (189) (315) (16.00)
1500 375 1338 413 5.00
CL00 - 0.275 0.22
(890) (222) (793) (245) (24.70)
C 1800 450 840 495 3.0
CL20 - 0.275 0.22
(1067) (267) (498) (294) (17.29)
1500 375 1411 375 6.00
D DL00 - 0.25 0.20
(890) (222) (837) (222) (29.64)
1500 375 1347 200 375 6.00
E EL00 0.25 0.20
(890) (222) (799) (119) (222) (29.64)

2010 Concrete Sustainability Conference 11 © National Ready Mixed Concrete Association


Table 5. Compressive strength of UHSC mixtures

Compressive strength, psi (MPa)


Mixture details 7 days 14 days 28 days
4 x 8 in. 4 x 8 in. 4 x 8 in.
2 in. 2 in. 2 in.
W/C (100 x (100 x (100 x
Category Mixture W/(C+SF) (50 mm) (50 mm) (50 mm)
ratio 200 mm) 200 mm) 200 mm)
Cube Cube Cube
Cylinder Cylinder Cylinder
AL00 6940
A 0.28 - - - - - -
(MC) (47.86)
BL00 6880
B 0.37 0.28 - - - - -
(MC) ( 47.45)
BL20 7080 8090 9210
0.37 0.28 - - -
(MC) (48.83) (55.79) (63.52)
BL20 8430 8630 (9650)
0.37 0.28 - - -
(WB) ( 58.14) (59.52) (66.55)
CL00 14,080 14,250 16,250
C 0.275 0.22 - - -
(WB) (97.10) (98.28) (112.06)
CL20 13,560 14,360 15,200
0.275 0.22 - - -
(WB) (93.52) (99.03) (104.82)
CL00 14,380 16,500 17,120
0.275 0.22 - - -
(OV) (97.10) (113.79) (118.04)
DL00
13,030 13,750 17,750
D (WB) 0.25 0.20 - - -
(89.86) (94.83) (122.41)

DL00 22,210 23,480


0.25 0.20 - 20,010 - -
(OV) (153.17) 161.90
(138.55)
EL00 21,180 23,420 24,010
E 0.25 0.20 - - -
(OV) (146.06) (161.52) (165.60)

Table 6. Modulus of rupture (R) of UHSC mixtures at 7 days

w/c R, psi
Category Mixture w/(c+sf)
ratio (MPa)
AL00 1675
A 0.28 0.28
(MC) (11.55)
BL00 1450
B 0.37 0.28
(MC) (10.00)
DL00 1585
D 0.25 0.20
(OV) (10.93)
EL00 2655
E 0.25 0.20
(OV) (18.31)

2010 Concrete Sustainability Conference 12 © National Ready Mixed Concrete Association


Figure 1. Relative gain of compressive strength.

Figure 2. Compressive strengths of plain and fiber reinforced UHSC.

2010 Concrete Sustainability Conference 13 © National Ready Mixed Concrete Association

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