- Reinforced concrete
Reinforced concrete is concrete in which reinforcement bars ("rebars"), reinforcement grids, plates or fibers have been incorporated to strengthen the concrete in tension. It was invented by French gardener Joseph Monier in 1849 and patented in 1867. The term Ferro Concrete refers only to concrete that is reinforced with iron or steel. Other materials used to reinforce concrete can be organic and inorganic fibres as well as composites in different forms. Prior to the invention of reinforcement, concrete was strong in compression, but weak in tension. Adding reinforcement crucially increases the strength in tension. The failure strain of concrete in tension is so low that the reinforcement has to hold the cracked sections together.
For a strong, ductile and durable construction the reinforcement needs to have the following properties:
- High strength
- High tensile strain
- Good bond to the concrete
- Thermal compatibility
- Durability in the concrete environment
In most cases reinforced concrete uses steel rebars that have been inserted to add strength.
Use in construction
Concrete is reinforced to give it extra tensile strength; without reinforcement, many concrete buildings would not have been possible.
Reinforced concrete can encompass many types of structures and components, including slabs, walls, beams, columns, foundations, frames and more.
Reinforced concrete can be classified as precast or cast in-situ concrete.
Much of the focus on reinforcing concrete is placed on floor systems. Designing and implementing the most efficient floor system is key to creating optimal building structures. Small changes in the design of a floor system can have significant impact on material costs, construction schedule, ultimate strength, operating costs, occupancy levels and end use of a building.
Behavior of reinforced concrete
Concrete is a mixture of Coarse (stone or brick chips) and Fine (generally sand) aggregates with a binder material(usually Portland cement). When mixed with a small amount of water, the cement hydrates to form microscopic opaque crystal lattices encapsulating and locking the aggregate into a rigid structure. Typical concrete mixes have high resistance to compressive stresses (about 4,000 psi (28 MPa)); however, any appreciable tension (e.g., due to bending) will break the microscopic rigid lattice, resulting in cracking and separation of the concrete. For this reason, typical non-reinforced concrete must be well supported to prevent the development of tension.
If a material with high strength in tension, such as steel, is placed in concrete, then the composite material, reinforced concrete, resists not only compression but also bending and other direct tensile actions. A reinforced concrete section where the concrete resists the compression and steel resists the tension can be made into almost any shape and size for the construction industry.
Three physical characteristics give reinforced concrete its special properties.
First, the coefficient of thermal expansion of concrete is similar to that of steel, eliminating large internal stresses due to differences in thermal expansion or contraction.
Second, when the cement paste within the concrete hardens this conforms to the surface details of the steel, permitting any stress to be transmitted efficiently between the different materials. Usually steel bars are roughened or corrugated to further improve the bond or cohesion between the concrete and steel.
Third, the alkaline chemical environment provided by the alkali reserve (KOH, NaOH) and the portlandite (calcium hydroxide) contained in the hardened cement paste causes a passivating film to form on the surface of the steel, making it much more resistant to corrosion than it would be in neutral or acidic conditions. When the cement paste exposed to the air and meteoric water reacts with the atmospheric CO2, portlandite and the Calcium Silicate Hydrate (CSH) of the hardened cement paste become progressively carbonated and the high pH gradually decreases from 13.5 – 12.5 to 8.5, the pH of water in equilibrium with calcite (calcium carbonate) and the steel is no longer passivated.
As a rule of thumb, only to give an idea on orders of magnitude, steel is protected at pH above ~11 but starts to corrode below ~10 depending on steel characteristics and local physico-chemical conditions when concrete becomes carbonated. Carbonation of concrete along with chloride ingress are amongst the chief reasons for the failure of reinforcement bars in concrete.
The relative cross-sectional area of steel required for typical reinforced concrete is usually quite small and varies from 1% for most beams and slabs to 6% for some columns. Reinforcing bars are normally round in cross-section and vary in diameter. Reinforced concrete structures sometimes have provisions such as ventilated hollow cores to control their moisture & humidity.
Distribution of concrete (in spite of reinforcement) strength characteristics along the cross-section of vertical reinforced concrete elements is inhomogeneous.
Mechanism of composite action of reinforcement and concrete
The reinforcement in a RC structure, such as a steel bar, has to undergo the same strain or deformation as the surrounding concrete in order to prevent discontinuity, slip or separation of the two materials under load. Maintaining composite action requires transfer of load between the concrete and steel. The direct stress is transferred from the concrete to the bar interface so as to change the tensile stress in the reinforcing bar along its length. This load transfer is achieved by means of bond (anchorage) and is idealized as a continuous stress field that develops in the vicinity of the steel-concrete interface.
Anchorage (bond) in concrete: Codes of specifications
Because the actual bond stress varies along the length of a bar anchored in a zone of tension, current international codes of specifications use the concept of development length rather than bond stress. The main requirement for safety against bond failure is to provide a sufficient extension of the length of the bar beyond the point where the steel is required to develop its yield stress and this length must be at least equal to its development length. However, if the actual available length is inadequate for full development, special anchorages must be provided, such as cogs or hooks or mechanical end plates. The same concept applies to lap splice length mentioned in the codes where splices (overlapping) provided between two adjacent bars in order to maintain the required continuity of stress in the splice zone.
In wet and cold climates, reinforced concrete for roads, bridges, parking structures and other structures that may be exposed to deicing salt may benefit from use of epoxy-coated, hot dip galvanised or stainless steel rebar, although good design and a well-chosen cement mix may provide sufficient protection for many applications. Epoxy coated rebar can easily be identified by the light green colour of its epoxy coating. Hot dip galvanized rebar may be bright or dull grey depending on length of exposure, and stainless rebar exhibits a typical white metallic sheen that is readily distinguishable from carbon steel reinforcing bar. Reference ASTM standard specifications A767 Standard Specification for Hot Dip Galvanised Reinforcing Bars, A775 Standard Specification for Epoxy Coated Steel Reinforcing Bars and A955 Standard Specification for Deformed and Plain Stainless Bars for Concrete Reinforcement.
Another, cheaper way of protecting rebars is coating them with zinc phosphate. Zinc phosphate slowly reacts with calcium cations and the hydroxyl anions present in the cement pore water and forms a stable hydroxyapatite layer.
Penetrating sealants typically must be applied some time after curing. Sealants include paint, plastic foams, films and aluminum foil, felts or fabric mats sealed with tar, and layers of bentonite clay, sometimes used to seal roadbeds.
Corrosion inhibitors, such as calcium nitrite [Ca(NO2)2], can also be added to the water mix before pouring concrete. Generally, 1–2 wt. % of [Ca(NO2)2] with respect to cement weight is needed to prevent corrosion of the rebars. The nitrite anion is a mild oxidizer that oxidizes the soluble and mobile ferrous ions (Fe2+) present at the surface of the corroding steel and causes it to precipitate as an insoluble ferric hydroxide (Fe(OH)3). This causes the passivation of steel at the anodic oxidation sites. Nitrite is a much more active corrosion inhibitor than nitrate, a less powerful oxidizer of the divalent iron.
Reinforcement and terminology of Beams
A beam bends under bending moment, resulting in a small curvature. At the outer face (tensile face) of the curvature the concrete experiences tensile stress, while at the inner face (compressive face) it experiences compressive stress.
A singly reinforced beam is one in which the concrete element is only reinforced near the tensile face and the reinforcement, called tension steel, is designed to resist the tension.
A doubly reinforced beam is one in which besides the tensile reinforcement the concrete element is also reinforced near the compressive face to help the concrete resist compression. The latter reinforcement is called compression steel. When the compression zone of a concrete is inadequate to resist the compressive Moment(positive moment), extra reinforcement has to be provided if the architect limits the dimensions of the section.
An under-reinforced beam is one in which the tension capacity of the tensile reinforcement is smaller than the combined compression capacity of the concrete and the compression steel (under-reinforced at tensile face). When the reinforced concrete element is subject to increasing bending moment, the tension steel yields while the concrete does not reach its ultimate failure condition. As the tension steel yields and stretches, an "under-reinforced" concrete also yields in a ductile manner, exhibiting a large deformation and warning before its ultimate failure. In this case the yield stress of the steel governs the design.
An over-reinforced beam is one in which the tension capacity of the tension steel is greater than the combined compression capacity of the concrete and the compression steel (over-reinforced at tensile face). So the "over-reinforced concrete" beam fails by crushing of the compressive-zone concrete and before the tension zone steel yields, which does not provide any warning before failure as the failure is instantaneous.
A balanced-reinforced beam is one in which both the compressive and tensile zones reach yielding at the same imposed load on the beam, and the concrete will crush and the tensile steel will yield at the same time. This design criterion is however as risky as over-reinforced concrete, because failure is sudden as the concrete crushes at the same time of the tensile steel yields, which gives a very little warning of distress in tension failure.
Steel-reinforced concrete moment-carrying elements should normally be designed to be under-reinforced so that users of the structure will receive warning of impending collapse.
The characteristic strength is the strength of a material where less than 5% of the specimen shows lower strength.
The design strength or nominal strength is the strength of a material, including a material-safety factor. The value of the safety factor generally ranges from 0.75 to 0.85 in Allowable Stress Design.
The ultimate limit state is the theoretical failure point with a certain probability. It is stated under factored loads and factored resistances.
Prestressed ConcreteMain article: Prestressed concrete
Prestressed concrete is a technique that greatly increases loadbearing strength of concrete beams. The reinforcing steel in the bottom part of the beam, which will be subjected to tensile forces when in service, is placed in tension prior to the concrete being poured around it. Once the concrete has hardened, the tension on the reinforcing steel is released, placing a built-in compressive force on the concrete. When loads are applied, the reinforcing steel takes on more stress and the compressive force in the concrete is reduced, but does not become a tensile force. Since the concrete is always under compression, it is less subject to cracking and failure.
Common failure modes of steel reinforced concrete
Reinforced concrete can fail due to inadequate strength, leading to mechanical failure, or due to a reduction in its durability. Corrosion and freeze/thaw cycles may damage poorly designed or constructed reinforced concrete. When rebar corrodes, the oxidation products (rust) expand and tends to flake, cracking the concrete and unbonding the rebar from the concrete. Typical mechanisms leading to durability problems are discussed below.
Cracking of the concrete section can not be prevented; however, the size of and location of the cracks can be limited and controlled by reinforcement, placement of control joints, the curing methodology and the mix design of the concrete. Cracking defects can allow moisture to penetrate and corrode the reinforcement. This is a serviceability failure in limit state design. Cracking is normally the result of an inadequate quantity of rebar, or rebar spaced at too great a distance. The concrete then cracks either under excess loading, or due to internal effects such as early thermal shrinkage when it cures.
Ultimate failure leading to collapse can be caused by crushing of the concrete, when compressive stresses exceed its strength; by yielding or failure of the rebar, when bending or shear stresses exceed the strength of the reinforcement; or by bond failure between the concrete and the rebar.
CarbonatationMain article: carbonatation
Carbonatation, or neutralisation, is a chemical reaction between carbon dioxide in the air with calcium hydroxide and hydrated calcium silicate in the concrete.
When designing a concrete structure, it is normal to state the concrete cover for the rebar (the depth within the object that the rebar will be). The minimum concrete cover is normally regulated by design or building codes. If the reinforcement is too close to the surface, early failure due to corrosion may occur. The concrete cover depth can be measured with a cover meter. However, carbonatated concrete only becomes a durability problem when there is also sufficient moisture and oxygen to cause electro-potential corrosion of the reinforcing steel.
One method of testing a structure for carbonatation is to drill a fresh hole in the surface and then treat the cut surface with phenolphthalein indicator solution. This solution will turn [pink] when in contact with alkaline concrete, making it possible to see the depth of carbonatation. An existing hole is no good because the exposed surface will already be carbonatated.
Chlorides, including sodium chloride, can promote the corrosion of embedded steel rebar if present in sufficienty high concentration. Chloride anions induce both localized corrosion (pitting corrosion) and generalized corrosion of steel reinforcements. For this reason, one should only use fresh raw water or potable water for mixing concrete, ensure that the coarse and fine aggregates do not contain chlorides, and not use admixtures that contain chlorides.
It was once common for calcium chloride to be used as an admixture to promote rapid set-up of the concrete. It was also mistakenly believed that it would prevent freezing. However, this practice has fallen into disfavor once the deleterious effects of chlorides became known. It should be avoided when ever possible.
The use of de-icing salts on roadways, used to reduce the freezing point of water, is probably one of the primary causes of premature failure of reinforced or prestressed concrete bridge decks, roadways, and parking garages. The use of epoxy-coated reinforcing bars and the application of cathodic protection has mitigated this problem to some extent. Also FRP rebars are known to be less susceptible to chlorides. Properly designed concrete mixtures that have been allowed to cure properly are effectively impervious to the effects of deicers.
Another important source of chloride ions is from sea water. Sea water contains by weight approximately 3.5 wt.% salts. These salts include sodium chloride, magnesium sulfate, calcium sulfate, and bicarbonates. In water these salts dissociate in free ions (Na+, Mg2+, Cl-, SO42-, HCO3-) and migrate with the water into the capillaries of the concrete. Chloride ions are particularly aggressive for the corrosion of the carbon steel reinforcement bars and make up about 50% of these ions.
In the 1960's and 1970's it was also relatively common for Magnesite, a chloride rich carbonate mineral, to be used as a floor-topping material. This was done principally as a levelling and sound attenuating layer. However it is now known that when these materials came into contact with moisture it produced a weak solution of hydrochloric acid due to the presence of chlorides in the magnesite. Over a period of time (typically decades) the solution caused corrosion of the embedded steel rebars. This was most commonly found in wet areas or areas repeatedly exposed to moisture.
Alkali silica reactionMain article: Alkali Silica Reaction
This a reaction of amorphous silica (chalcedony, chert, siliceous limestone) sometimes present in the aggregates with the hydroxyl ions (OH-) from the cement pore solution. Poorly crystallized silica (SiO2) dissolves and dissociates at high pH (12.5 - 13.5) in alkaline water. The soluble dissociated silicic acid reacts in the porewater with the calcium hydroxide (portlandite) present in the cement paste to form an expansive calcium silicate hydrate (CSH). The alkali silica reaction (ASR), causes localised swelling responsible of tensile stress and cracking. The conditions required for alkali silica reaction are threefold: (1) aggregate containing an alkali-reactive constituent (amorphous silica), (2) sufficient availability of hydroxyl ions (OH-), and (3) sufficient moisture, above 75 % relative humidity (RH) within the concrete. This phenomenon is sometimes popularly referred to as "concrete cancer". This reaction occurs independently of the presence of rebars: massive concrete structures such as dams can be affected.
Conversion of high alumina cement
Resistant to weak acids and especially sulfates, this cement cures quickly and reaches very high durability and strength. It was greatly used after World War II for making precast concrete objects. However, it can lose strength with heat or time (conversion), especially when not properly cured. With the collapse of three roofs made of prestressed concrete beams using high alumina cement, this cement was banned in the UK in 1976. Subsequent inquiries into the matter showed that the beams were improperly manufactured, but the ban remained.
Sulphates (SO4) in the soil or in groundwater, in sufficient concentration, can react with the Portland cement in concrete causing the formation of expansive products, e.g. ettringite or thaumasite, which can lead to early failure of the structure. The most typical attack of this type is on concrete slabs and foundation walls at grade where the sulfate ion, via alternate wetting and drying, can increase in concentration. As the concentration increases, the attack on the Portland cement can begin. For buried structures such as pipe, this type of attack is much rarer especially in the Eastern half of the United States. The sulfate ion concentration increases much slower in the soil mass and is especially dependent upon the initial amount of sulfates in the native soil. The chemical analysis of soil borings should be done during the design phase of any project involving concrete in contact with the native soil to check for the presence of sulfates. If the concentrations are found to be aggressive, various protective coatings can be used. Also, in the US ASTM C150 Type 5 Portland cement can be used in the mix. This type of cement is designed to be particularly resistant to a sulfate attack.
Steel plate constructionMain article: Steel plate construction
In steel plate construction, stringers join parallel steel plates. The plate assemblies are fabricated off site, and welded together on-site to form steel walls connected by stringers. The walls become the form into which concrete is poured. Steel plate construction speeds reinforced concrete construction by cutting out the time consuming on-site manual steps of tying rebar and building forms. The method has excellent strength because the steel is on the outside, where tensile forces are often greatest.
Fiber-reinforced concreteMain article: Fiber reinforced concrete
Fiber reinforcement is mainly used in shotcrete, but can also be used in normal concrete. Fiber-reinforced normal concrete is mostly used for on-ground floors and pavements, but can be considered for a wide range of construction parts (beams, pillars, foundations, etc.), either alone or with hand-tied rebars.
Concrete reinforced with fibers (which are usually steel, glass, or plastic fibers) is less expensive than hand-tied rebar, while still increasing the tensile strength many times. Shape, dimension, and length of fiber are important. A thin and short fiber, for example short, hair-shaped glass fiber, will only be effective the first hours after pouring the concrete (reduces cracking while the concrete is stiffening) but will not increase the concrete tensile strength. A normal-size fiber for European shotcrete (1 mm diameter, 45 mm length—steel or plastic) will increase the concrete's tensile strength.
Steel is the strongest commonly-available fiber, and comes in different lengths (30 to 80 mm in Europe) and shapes (end-hooks). Steel fibers can only be used on surfaces that can tolerate or avoid corrosion and rust stains. In some cases, a steel-fiber surface is faced with other materials.
Glass fiber is inexpensive and corrosion-proof, but not as ductile as steel. Recently, spun basalt fiber, long available in Eastern Europe, has become available in the U.S. and Western Europe. Basalt fibre is stronger and less expensive than glass, but historically has not resisted the alkaline environment of portland cement well enough to be used as direct reinforcement. New materials use plastic binders to isolate the basalt fiber from the cement.
The premium fibers are graphite-reinforced plastic fibers, which are nearly as strong as steel, lighter-weight, and corrosion-proof. Some experiments have had promising early results with carbon nanotubes, but the material is still far too expensive for any building.
There is considerable overlap between the subjects of non-steel reinforcement and fiber-reinforcment of concrete. The introduction of non-steel reinforcement of concrete is relatively recent; it takes two major forms: non-metallic rebar rods, and non-steel (usually also non-metallic) fibres incorporated into the cement matrix. For example there is increasing interest in glass fiber reinforced concrete (GFRC) and in various applications of polymer fibres incorporated into concrete. Although currently there is not much suggestion that such materials will in general replace metal rebar, some of them have major advantages in specific applications, and there also are new applications in which metal rebar simply is not an option. However, the design and application of non-steel reinforcing is fraught with challenges; for one thing, concrete is a highly alkaline environment, in which many materials, including most kinds of glass, have a poor service life. Also, the behaviour of such reinforcing materials differ from the behaviour of metals, for instance in terms of shear strength, creep and elasticity.
Fibre-Reinforced Polymer (FRP) (Fibre-reinforced plastic or FRP) and Glass-reinforced plastic (GRP) consist of fibres of polymer, glass, carbon, aramid or other polymers or high-strength fibres set in a resin matrix to form a rebar rod or grid or fibres. These rebars are installed in much the same manner as steel. The cost is higher but, suitably applied, the structures have advantages, in particular a dramatic reduction in problems related to corrosion, either by intrinsic concrete alkalinity or by external corrosive fluids that might penetrate the concrete. These structures can be significantly lighter and usually have a longer service life. The cost of these materials has dropped dramatically since their widespread adoption in the aerospace industry and by the military.
In particular FRP rods are useful for structures where the presence of steel would not be acceptable. For example, MRI machines have huge magnets, and accordingly require non-magnetic buildings. Again, toll booths that read radio tags need reinforced concrete that is transparent to radio. Also, where the design life of the concrete structure is more important than its initial costs, non-steel reinforcing often has its advantages where corrosion of reinforcing steel is a major cause of failure. In such situations corrosion-proof reinforcing can extend a structure's life substantially, for example in the intertidal zone. FRP rods may also be useful in situations where it is likely that the concrete structure may be compromised in future years, for example the edges of balconies when balustrades are replaced and bathroom floors in multi-story construction where the service life of the floor structure is likely to be many times the service life of the waterproofing building membrane.
Plastic reinforcement often is stronger, or at least has a better strength to weight ratio than reinforcing steels. Also, because it resists corrosion, it does not need a protective concrete cover as thick as steel reinforcement does (typically 30 to 50 mm or more). FRP-reinforced structures therefore can be lighter and last longer. Accordingly, for some applications the whole-life cost will be price-competitive with steel-reinforced concrete.
The material properties of FRP or GRP bars differ markedly from steel, so there are differences in the design considerations. FRP or GRP bars have relatively higher tensile strength but lower stiffness, so that Deflections are likely to be higher than for equivalent steel-reinforced units. Structures with internal FRP reinforcement typically have an elastic deformability comparable to the plastic deformability (ductility) of steel reinforced structures. Failure in either case is more likely to occur by compression of the concrete than by rupture of the reinforcement. Deflection is always a major design consideration for reinforced concrete. Deflection limits are set to ensure that crack widths in steel-reinforced concrete are controlled to prevent water, air or other aggressive substances reaching the steel and causing corrosion. For FRP-reinforced concrete, aesthetics and possibly water-tightness will be the limiting criteria for crack width control. FRP rods also have relatively lower compressive strengths than steel rebar, and accordingly require different design approaches for columns.
One drawback to the use of FRP reinforcement is the limited fire resistance. Where fire safety is a consideration, structures employing FRP have to maintain their strength and the anchoring of the forces at temperatures to be expected in the event of fire. For purposes of fireproofing an adequate thickness of cement concrete cover or protective cladding is necessary. The disadvantages are not on the side of the FRP however, addition of 1kg/m3 of polypropylene fibers to concrete has been shown to reduce spalling during a simulated fire. (The improvement is thought to be due to the formation of pathways out of the bulk of the concrete, allowing steam pressure to dissipate.)
Another problem is the effectiveness of shear reinforcement. FRP rebar stirrups formed by bending before hardening generally perform relatively poorly in comparison to steel stirrups or to structures with straight fibres. When strained, the zone between the straight and curved regions are subject to strong bending, shear, and longitudinal stresses. Special design techniques are necessary to deal with such problems.
There is growing interest in application of external reinforcement of existing structures with advanced materials such as carbon fibre, that can impart exceptional strength.
- Concrete protection
- Cover Meter
- Concrete cover
- Types of concrete
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- Composite materials
- Structural engineering
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