Introduction To Construction Materials: and Testing
Introduction To Construction Materials: and Testing
Construction Materials
and Testing
Factors that affect the choice of materials for a
particular scheme:
• Climatic background - different materials and forms of construction have
developed in different parts of the world as a result of climatic differences;
strength at low and high temperatures, resistance to ordinary water and sea
water, acids and alkalis etc.
• Economic aspect - The rapid advance of constructional methods, the
increasing introduction of mechanical tools and plants, and changes in the
organisation of the building industry may appreciably influence the choice of
materials.
PROPERTIES OF CONSTRUCTION
MATERIALS:
PHYSICAL PROPERTIES
•
•
•
• Weathering Resistance is the ability of a material to endure alternate wet
and dry conditions for a long period without considerable deformation and
loss of mechanical strength.
• Water Permeability is the capacity of a material to allow water to penetrate
under pressure. Materials like glass, steel and bitumen are impervious.
• Frost Resistance denotes the ability of a water-saturated material to endure
repeated freezing and thawing with considerable decrease of mechanical
strength. Under such conditions the water contained by the pores increases
in volume even up to 9 per cent on freezing. Thus the walls of the pores
experience considerable stresses and may even fail.
• Heat Conductivity is the ability of a material to conduct heat. It is
influenced by nature of material, its structure, porosity, character of pores
and mean temperature at which heat exchange takes place. Materials with
large size pores have high heat conductivity because the air inside the pores
enhances heat transfer. Moist materials have a higher heat conductivity than
drier ones. This property is of major concern for materials used in the walls
of heated buildings since it will affect dwelling houses.
• Thermal Capacity is the property of a material to absorb heat described by
its specific heat. Thermal capacity is of concern in the calculation of thermal
stability of walls of heated buildings and heating of a material, e.g. for
concrete laying in winter.
• Fire Resistance is the ability of a material to resist the action of high
temperature without any appreciable deformation and substantial loss of
strength. Fire resistive materials are those which char, smoulder, and ignite
with difficulty when subjected to fire or high temperatures for long period
but continue to burn or smoulder only in the presence of flame, e.g. wood
impregnated with fire proofing chemicals. Non-combustible materials neither
smoulder nor char under the action of temperature. Some of the materials
neither crack nor lose shape such as clay bricks, whereas some others like
steel suffer considerable deformation under the action of high temperature.
• Refractoriness denotes the ability of a material to withstand prolonged
action of high temperature without melting or losing shape. Materials
resisting prolonged temperatures of 1580°C or more are known as refractory.
High-melting materials can withstand temperature from 1350–1580°C,
whereas low-melting materials withstand temperature below 1350°C.
• Chemical Resistance is the ability of a material to withstand the action of
acids, alkalis, sea water and gases. Natural stone materials, e.g. limestone,
marble and dolomite are eroded even by weak acids, wood has low resistance
to acids and alkalis, and bitumen disintegrates under the action of alkali
liquors.
• Durability is the ability of a material to resist the combined effects of
atmospheric and other factors.
CE 3102 Course Outline
Building materials have an important role to play in this modern age of technology. Although
their most important use is in construction activities, no field of engineering is conceivable without their
use. Also, the building materials industry is an important contributor in our national economy as its output
governs both the rate and the quality of construction work.
Factors that affect the choice of materials for a particular scheme:
• Climatic background - different materials and forms of construction have developed in
different parts of the world as a result of climatic differences; strength at low and high temperatures,
resistance to ordinary water and sea water, acids and alkalis etc.
• Economic aspect - The rapid advance of constructional methods, the increasing
introduction of mechanical tools and plants, and changes in the organisation of the building industry may
appreciably influence the choice of materials.
PHYSICAL PROPERTIES
A
where M = mass (g)
V = volume (cm3)
2. Bulk Density (ρb) is the mass of a unit volume of material in its natural state (with pores and
voids) calculated as
4. Specific Density (ɣ) also known as the unit weight) is the weight per unit volume of material,
where ɣ = specific weight (kN/m3)
ρ = density of the material (kg/m)
g = gravity (m/s2)
5. Specific Gravity (Gs) of solid particles of a material is the ratio of weight/mass of a given
volume of solids to the weight/mass of an equal volume of water at 4°C.
7. Apparent or Mass Specific Gravity (Gm) If both the permeable and impermeable voids are
included to determine the true volume of solids, the specific gravity is called apparent specific
gravity. It is the ratio of mass density of fine grained material to the mass density of water.
8. Porosity (n) is the degree to which volume of the material of the material is interspersed with
pores. It is expressed as a ratio of the volume of pores to that of the specimen.
Following inter relationship exists between void ratio and the porosity.
9. Void Ratio (e) is defined as the ratio of volume of voids (Vv) to the volume of solids (Vs).
10. Hygroscopicity is the property of a material to absorb water vapour from air. It is influenced by
air-temperature and relative humidity; pores—their types, number and size, and by the nature of
substance involved.
11. Water Absorption denotes the ability of the material to absorb and retain water. It is expressed
as percentage in weight or of the volume of dry material:
13. Water Permeability is the capacity of a material to allow water to penetrate under pressure.
Materials like glass, steel and bitumen are impervious.
14. Frost Resistance denotes the ability of a water-saturated material to endure repeated freezing
and thawing with considerable decrease of mechanical strength. Under such conditions the water
contained by the pores increases in volume even up to 9 per cent on freezing. Thus the walls of
the pores experience considerable stresses and may even fail.
15. Heat Conductivity is the ability of a material to conduct heat. It is influenced by nature of
material, its structure, porosity, character of pores and mean temperature at which heat exchange
takes place. Materials with large size pores have high heat conductivity because the air inside the
pores enhances heat transfer. Moist materials have a higher heat conductivity than drier ones.
This property is of major concern for materials used in the walls of heated buildings since it will
affect dwelling houses.
16. Thermal Capacity is the property of a material to absorb heat described by its specific heat.
Thermal capacity is of concern in the calculation of thermal stability of walls of heated buildings
and heating of a material, e.g. for concrete laying in winter.
17. Fire Resistance is the ability of a material to resist the action of high temperature without any
appreciable deformation and substantial loss of strength. Fire resistive materials are those which
char, smoulder, and ignite with difficulty when subjected to fire or high temperatures for long
period but continue to burn or smoulder only in the presence of flame, e.g. wood impregnated
with fire proofing chemicals. Non-combustible materials neither smoulder nor char under the
action of temperature. Some of the materials neither crack nor lose shape such as clay bricks,
whereas some others like steel suffer considerable deformation under the action of high
temperature.
18. Refractoriness denotes the ability of a material to withstand prolonged action of high
temperature without melting or losing shape. Materials resisting prolonged temperatures of
1580°C or more are known as refractory. High-melting materials can withstand temperature from
1350–1580°C, whereas low-melting materials withstand temperature below 1350°C.
19. Chemical Resistance is the ability of a material to withstand the action of acids, alkalis, sea
water and gases. Natural stone materials, e.g. limestone, marble and dolomite are eroded even by
weak acids, wood has low resistance to acids and alkalis, and bitumen disintegrates under the
action of alkali liquors.
20. Durability is the ability of a material to resist the combined effects of atmospheric and other
factors.
The important mechanical properties considered for building materials are: strength, compressive,
tensile, bending, impact, hardness, plasticity, elasticity, and abrasion resistance.
1. Strength is the ability of the material to resist failure under the action of stresses caused by loads,
the most common being compression, tension, bending and impact. The importance of studying
the various strengths will be highlighted from the fact that materials such as stones and concrete
have high compressive strength but a low (1/5 to 1/50) tensile, bending and impact strengths.
Compressive Strength is found from tests on standard cylinders, prisms and cubes—smaller for
homogeneous materials and larger for less homogeneous ones. Prisms and cylinders have lower
resistance than cubes of the same cross-sectional area, on the other hand prisms with heights
smaller than their sides have greater strength than cubes. This is due to the fact that when a
specimen is compressed the platens of the compression testing machine within which the
specimen is placed, press tight the bases of the specimen and the resultant friction forces prevent
the expansion of the adjoining faces, while the central lateral parts of the specimen undergoes
transversal expansion. The only force to counteract this expansion is the adhesive force between
the particles of the material. That is why a section away from the press plates fails early.
The test specimens of metals for tensile strength are round bars or strips and that of binding
materials are of the shape of figure eight.
Bending Strength tests are performed on small bars (beams) supported at their ends and subjected
to one or two concentrated loads which are gradually increased until failure takes place.
2. Hardness is the ability of a material to resist penetration by a harder body. Mohs scale is used to
find the hardness of materials. It is a list of ten minerals arranged in the order of increasing
hardness (Section 3.2). Hardness of metals and plastics is found by indentation of a steel ball.
3. Elasticity is the ability of a material to restore its initial form and dimensions after the load is
removed. Within the limits of elasticity of solid bodies, the deformation is proportional to the
stress. Ratio of unit stress to unit deformation is termed as modulus of elasticity. A large value of
it represents a material with very small deformation.
4. Plasticity is the ability of a material to change its shape under load without cracking and to retain
this shape after the load is removed. Some of the examples of plastic materials are steel, copper
and hot bitumen.
Brittleness
- Brittle materials have little or no plasticity. They fail suddenly without warning. Cast iron,
stone, brick and concrete are comparatively brittle materials having a considerable amount of
plasticity.
Stiffness
- Stiff materials have a high modulus of elasticity permitting small deformation for a given
load.
Flexibility
- Flexible materials on the other hand have low modulus of elasticity and bend considerably
without breakdown.
Toughness
- Tough materials withstand heavy shocks. Toughness depends upon strength and flexibility.
Malleability
- Malleable materials can be hammered into sheets without rupture. It depends upon ductility
and softness of material. Copper is the most malleable material.
Hardness
- Hard materials resist scratching and denting, for example cast iron and chrome steel.
Materials resistant to abrasion such as manganese are also known as hard materials.
MECHANICAL
PROPERTIES
The important mechanical properties considered for building materials are:
strength, compressive, tensile, bending, impact, hardness, plasticity, elasticity,
and abrasion resistance.
• Strength is the ability of the material to resist failure under the action of
stresses caused by loads, the most common being compression, tension,
bending and impact. The importance of studying the various strengths will be
highlighted from the fact that materials such as stones and concrete have
high compressive strength but a low (1/5 to 1/50) tensile, bending and
impact strengths.
• Hardness is the ability of a material to resist penetration by a harder body.
Mohs scale is used to find the hardness of materials. It is a list of ten minerals
arranged in the order of increasing hardness (Section 3.2). Hardness of
metals and plastics is found by indentation of a steel ball.
• Elasticity is the ability of a material to restore its initial form and dimensions
after the load is removed. Within the limits of elasticity of solid bodies, the
deformation is proportional to the stress. Ratio of unit stress to unit
deformation is termed as modulus of elasticity. A large value of it represents a
material with very small deformation.
• Plasticity is the ability of a material to change its shape under load without
cracking and to retain this shape after the load is removed. Some of the
examples of plastic materials are steel, copper and hot bitumen.
CHARACTERISTIC BEHAVIOUR
UNDER STRESS
Common characteristics of building materials under stress:
• Ductility - The ductile materials can be drawn out without necking down, the
examples being copper and wrought iron.
• Brittleness - Brittle materials have little or no plasticity. They fail suddenly
without warning. Cast iron, stone, brick and concrete are comparatively
brittle materials having a considerable amount of plasticity.
• Stiffness - Stiff materials have a high modulus of elasticity permitting small
deformation for a given load.
• Flexibility - Flexible materials on the other hand have low modulus of
elasticity and bend considerably without breakdown.
• Toughness -Tough materials withstand heavy shocks. Toughness depends
upon strength and flexibility.
• Malleability - Malleable materials can be hammered into sheets without
rupture. It depends upon ductility and softness of material. Copper is the
most malleable material.
• Hardness -Hard materials resist scratching and denting, for example cast
iron and chrome steel. Materials resistant to abrasion such as manganese are
also known as hard materials.
CE 3102 Course Outline
Hydrometer Analysis
Particle Size Distribution of Soils Test, ASTM D422
Hydrometer analysis provides a quantitative evaluation of
the particle-size distribution of the material that is smaller
than 75μm (No. 200 sieve) found in typical evaluations of
fine-grained soils. The test is used in conjunction with a
standard sieve analysis of fine-grained soils with a wide
range of particle sizes to provide a complete gradation
curve. It is also used to more accurately evaluate the
sedimentation or fines of a particular soil.
Hydrometer soil analysis is based on Stokes Law, which claims that the velocity at which a
particle settles while suspended, all other factors being equal, is determined by the shape, weight
and size of the particle. Because it is assumed that soil particles have the same specific gravity,
it’s expected that larger particles will settle more quickly than finer ones in a soil-water
suspension. By measuring suspended solids in sedimentation cylinders, hydrometers are able to
measure a soil’s particle-size distribution.
To perform a hydrometer analysis the test specimen is combined with a dispersing agent and test
water. This sample is then thoroughly mixed and placed into a cylinder with additional water. A
hydrometer is then used to take readings at specific time intervals. The results of this test can
then be combined with the sieve analysis to establish a complete gradation curve of the material
or used to just evaluate the sedimentation or fines of the material.
Hydrometer analysis requires several items. These include soil hydrometers, hydrometer jar
baths, constant-temperature water baths, soil dispersion mixers and sodium hexametaphosphate.
MOISTURE CONTENT OF SOIL
The water content of soil is a critical factor in the ability to
control compaction. Moisture analyzers and testers are able
to determine the water content of soil and other materials by
calculating the dry density of the soil or to ensure that the
water content is within the ideal range of compaction. The
testing information is also used to provide preliminary
results during a construction project to determine whether
water needs to be added or removed.
PERMEABILITY OF SOIL
Permeability Test of Soil
Soil permeability, in terms of a permeability coefficient
(k), measures a soil’s ability to allow water to pass through
it. Soils are permeable materials due to their grain structure
and the existence of interconnected voids. Materials with a
high permeability coefficient will allow fluids to move
rapidly through them while those with a low permeability
will not.
While testing permeability, it is important to make sure all specified conditions are met.
The discharged water must be under laminar flow conditions and move under a unit hydraulic
gradient at standard temperature conditions (20°C). Additionally, consistency of pressure is
important to maintain. Certain control products are useful in regulating the testing environment.
A permeability coefficient is most commonly determined through the use of two main
laboratory tests: the constant head permeability test and the falling head permeability test. For
highly granular soils such as sands and gravels, the constant head method is best and can yield
accurate results even if the sample has been disturbed or reconstituted. The falling head method
is typically used for fine-grained soils and is more accurate when testing undisturbed samples.
These two methods work in different ways to determine a sample’s permeability coefficient.
The constant head permeability test:
The constant head permeability test utilizes a test apparatus with a reservoir on the top to hold
de-aired water and one at the bottom to hold water that has permeated through the soil sample.
Because the samples are large-grained, their hydraulic conductivity is rather fast. The coefficient
of permeability can be calculated using the pressure measurements and volume of the permeated
water during the set time interval, as well as the height and cross-sectional area of the soil
sample. To ensure accurate results, repeat the test three or more times and find an
average coefficient.
The falling head permeability test:
The falling head permeability test is performed using a standpipe and a relatively small sample
size. A small sample size is due to the fine-grained nature of the test samples, which results in
slow hydraulic conductivity. The soil sample is first placed in a container and saturated with
water. From there, the sample is attached to standpipes filled with a specific level of de-aired
water. The permeability coefficient can be calculated when the water in the standpipe has
reached a previously determined level. The calculation takes into account the size of the sample,
the cross-sectional area of the standpipe, as well as the time it took to change the water level.
PH
Humboldt offers a variety of pH meters and accessories
as part of a complete line of soil laboratory testing
equipment. The HO-4960 pH Bench Meter with
Electrode offers premium features for cost-effective and
reliable pH and ORP measurements. It includes the HO-
4963 3-in-1 plastic refillable pH electrode, pH Buffer
Power Sachet and In-Use Cover.
The HO-4930 Portable pH Meter offers portability with
precise pH measuring capabilities. An ORP or temperature electrode can also be easily
connected for additional functionality. It includes the HO-4964 Plastic Gel, non-refillable
electrode and a pH buffer powder sachet.
Analysis and Conductivity Pens are also offered to measure different properties of the
sample. pH Buffer Solutions with 0.01 resolution are standardized against NIST-traceable pH
references at 77°F (25°C).
SAMPLE PREPARATION
Testing of soil for building construction or of any
structure should always be the first step in planning to
ensure the suitability of soil properties. The soil will need
to handle the stress emanating from the structure and any
unreliable or undetermined tests can be catastrophic to its
ultimate life span and safety.
The specific types of tests needed will depend on the
properties of the soil and the type of construction project.
Thorough understanding of soil properties can even sometimes enable engineers to build in
potentially problematic areas.
In order for soil samples to be correctly and thoroughly tested in the lab, they must first be
collected and processed. The soil samples need to be dried, ground and sieved before they are
analyzed. A number of different tools are employed for proper preparation of the soil samples for
testing. Soil grinders are used to prepare samples for evaluation of grain sizes, Atterberg Limits
and other tests. Soil mixers are designed to mechanically mix the sample with an in situ binder.
The process breaks up the soil, injects a binder at low pressure and mixes the binder with
the soil.
The Rapid Soil Processor simplifies preparing soil for compaction tests by producing five-point
moisture density test results five times faster than any other available method.
The Soil Grinder prepares samples to a designated particle size for accurate, repeatable results,
can grind a one-point sample in 15 seconds.
The Electric Disk Grinding Mill is used globally for sample. The grinding mill head and plates
are made with quality materials for durability and long service life. The grinding mill head is
easily removed and disassembled for cleaning.
The Hand-Operated Disk Grinding Mill mounts to a bench top with an integral c-clamp for fast
grinding of samples. The mill head is easily disassembled for cleaning without any special
tools needed.
The 5-Qt. Mixer thoroughly blends, mixes and aerates all ingredients for a consistent, predictable
result. Includes a stainless steel bowl, wire whip, dough hook and aluminum flat beater.
The Mortar Mixer (5L – 5.3 qt.) is a high-quality ASTM mixer that provides a more durable and
lower cost alternative to the Hobart mixer. It features a robust design and works especially well
for efficient mixing of cement pastes and mortar.
The heavy porcelain Soil Mortar is ASTM D421 compliant and specifically for use with our H-
4258 Soil Pestle.
The characteristics governing the behaviour of material when external forces are applied are
included in these properties. Some of the important mechanical properties are elasticity,
hardness, plasticity, strength, etc.
The properties of metals and alloys which have a bearing on their processing or application are
called technological properties. Castability, machinability, weldability and workability are some
of the significant technological properties of metals and alloys.
Out of all such properties, the physical properties and mechanical properties are particularly very
important to a construction engineer. Materials can be selected to withstand fluctuating and high
temperatures.
Physical Properties of Engineering Materials:
Following terms in connection with the physical properties of engineering materials are defined
and explained:
The technical properties of the material such as strength, heat, conductivity, etc. are greatly
influenced by its bulk density and hence the performance efficiency of a material will depend
upon its bulk density.
For most of the materials, the bulk density is less than its density except for dense materials,
liquids and materials obtained from the molten masses.
Table 1-1 shows the bulk densities of some of the important building materials.
(4) Density:
The term density of a material is defined as the mass of a unit volume of homogeneous material.
It is obtained by working out the ratio of mass of material to the volume of material in
homogeneous state. The physical properties of a material are greatly influenced by its density.
(6) Durability:
The property of a material to resist the combined action of atmospheric and other factors is
known as its durability.
The running or maintenance cost of a building will naturally depend upon the durability of the
materials of which it is composed.
(9) Hygroscopicity:
The property of a material to absorb water vapour from air is known as the hygroscopicity and it
is governed by the nature of substance involved, number of pores, air temperature, relative
humidity, etc. The water-retaining or hydrophilic substances readily dissolve in water.
(10) Porosity:
The term porosity is used to indicate the degree by which the volume of a material is occupied by
pores. It is expressed as a ratio of volume of pores to that of the specimen. The porosity of a
material is indicative of its various properties such as strength, bulk density, water absorption,
thermal conductivity, durability, etc., and hence it is to be carefully studied and analysed.
(11) Refractoriness:
The ability of a material to withstand prolonged action of high temperature without melting or
loosing shape is known as its refractoriness.
The property of a material to absorb heat is known as its thermal capacity and it is worked out by
the following equation –
T = H / M (T2 – T1)
Where, T = Thermal capacity in J/N °C
H = Quantity of heat required to increase the temperature of material from T1 to T2 in J
M = Mass of material in N
T1 = Temperature of material before heating in °C
T2 = Temperature of material after heating in °C.
(2) Creep:
In many applications, the building materials are required to sustain steady loads for long periods.
Under such conditions, the material may continue to deform until its usefulness is seriously
reduced. Such time-dependent deformations of a structure can grow large and may even result in
final fracture without any increase in load. If the deformation continues even when the load is
constant, such additional deformation is known as the creep.
Most of the building materials creep to a certain extent at all temperatures. However the
engineering metals such as steel, aluminium and copper creep very little at room temperature.
The high temperatures lead to rapid creep which is often accompanied by microstructural
changes. The phenomenon of creep is important in polymers at room temperature, in alloys of
aluminium at 100°C and in steels above 300°C.
(3) Elasticity:
When a load is applied to a material, there is change in its shape and dimension. The term
elasticity is used to indicate the ability of a material to restore its initial form and dimensions
after the load is removed.
The difference between the following two terms should be noted:
(i) Elastic Deformation:
A deformation is said to be elastic when the solid deforms when it is loaded but returns to its
original position when unloaded. A change in pressure or an application of load results in the
elastic deformation. The term ideal deformation is used to mean the deformation that takes place
instantaneously upon application of force and disappears completely on removal of the force.
Such deformations obey Hooke’s law and the elastic strain of the metal is directly proportional to
the applied force. The ideal deformation occurs with comparatively smaller deformation forces
which can keep the working stresses within the elastic limit.
(4) Fatigue:
When the materials are subjected to a repetitive or fluctuating stress, they will fail at a stress
much lower than that required to cause fracture under steady loads.
This behaviour is called the fatigue and it is distinguished by the following three features:
(i) Increased uncertainty in strength and service life;
(ii) Loss of ductility; and
(iii) Loss of strength.
(5) Hardness:
The ability of a material to resist penetration by a harder body is known as its hardness. It is a
major factor in deciding the workability and use of a material for floors and road surfaces. The
hardness is not a fundamental property. But it is a combined effect of compressive, elastic and
plastic properties relative to the mode of penetration, shape of penetrator, etc.
The hardness bears a fairly constant relationship to the tensile strength of a given material. It can
therefore be used as a practical non-destructive test to get roughly an idea of the tensile strength
of the material and the state of the metal near the surface.
The hardness of stone materials can be determined with the help of Mohs’ scale of hardness. It is
a list of ten materials arranged in the order of increasing hardness. The hardness of a material lies
between the hardness of two materials i.e. the one which scratches and the other which is
scratched by the material to be tested.
Table 1-2 shows the Mohs’ scale of hardness.
(6) Impact Strength:
The impact strength of a material is the quantity of work required to cause its failure per its unit
volume. It thus indicates the toughness of a material and the materials are tested in an impact
testing machine to determine their impact strength.
The impact strength is a complex characteristic which takes into account both the toughness and
strength of a material.
It varies with the following factors:
(i) If the dimensions of the specimen are increased, there is also increase in the impact strength.
(ii) If the sharpness of the notch increases, the impact strength required to cause failure
decreases.
(iii) The angle of the notch also improves the impact strength after certain values.
(iv) The impact strength is also affected to a certain extent by the velocity of impact.
(v) The temperature of the specimen under test gives an indication about the type of fracture that
is likely to occur i.e. ductile, brittle or ductile to brittle transition.
(8) Strength:
The ability of a material to resist failure under the action of stresses caused by a load is known as
its strength. The loads to which a material is commonly subjected to are compression, tension
and bending. The corresponding strength is obtained by dividing the ultimate load with the cross-
sectional area of the specimen.
The stresses in the building materials are not allowed to exceed a certain percentage of their
ultimate strength. Thus, a margin of safety is provided and the term factor of safety is used to
denote the ratio of ultimate stress to safe stress. For instance, if the factor of safety is two, the
stress to be adopted for design purposes would be one-half of the ultimate stress.
The values of factors of safety are specified by design standards and they are framed by taking
into account various factors such as nature of work, quality of material, service conditions,
economic considerations, etc.
(9) Wear:
The failure of a material under the combined actions of abrasion and impact is known as its wear.
The wear resistance is usually expressed as a percentage of loss in weight and it is of great
importance in deciding the suitability of a material for use of road surfaces, railway ballast, etc.
CE 3102 Course Outline
Specific Weight
- Also known as Unit Weight
- The bulk density or unit weight of an aggregate is the mass or weight of the aggregate
required to fill a container of a specified unit volume. The volume referred to here is that
occupied by both aggregates and the voids between aggregate particles.
Bulk density of aggregates depends upon the following 3 factors:
Degree of compaction
Grading of aggregates
Shape of aggregate particles
Water Absorption
- Aggregate can contain water, both internal, based on porosity, and external, surface
moisture. This gives aggregate the ability to absorb water. This will effectively reduce the
amount of water available for hydration; or conversely, if the aggregate is very wet, add
excess water to a cement mix.
- Is used to determine the amount of water absorbed under specified conditions.
- Water absorption of aggregates is the % of water absorbed by an air-dried aggregate
when immersed in water at 27°C for a period of 24 hours.
- The water absorption test use to find the water holding capacity of the aggregates.
- The water is absorbed by the aggregates or stones in their pores known as the water
absorption. Usually water absorption gives an idea about the strength of the aggregates.
Those aggregate has more water absorption is usually unsuitable for the construction.
Factors affecting water absorption include:
1. Type of plastic
2. Additives used
3. Temperature
4. Length of exposure.
Abrasion
- Is detachment of particles from material due to weak bond between particles. This can be
prevented by better bonding between particles. Example of abrasion is removal of stones
from bitumenous roads due to tyre friction.
Related theory:
Setting:
It is the measure of gain of stiffness of the cement paste. At this level paste acquires stable shape
and volume and does not flow under its weight on a mild slope surface.
In the setting process little chemical reaction takes place. It only includes the shape acquisition
due to evaporation of water. During the setting process the cement remains in the fluid or the
semi-fluid state and there is very little or no gain in strength. Finer the cement particles more will
be the hydration and therefore it will lead to quick settlement.
Hardening:
Hardening is the rate of gain of strength due to the chemical reaction. It also refers to the strength
of the concrete after a specified interval of time. It can take little load and will maintain its
acquired shape.
Initial setting time/ VICAT time of initial setting:
It is the time elapsed between the start of mixing of water in the cement to the condition of
cement paste such that 1 mm diameter needle of VICAT apparatus penetrates into the paste by
25 mm
Final setting time/ VICAT time of final setting:
It is the time from start of mixing (when water is added) till the condition of paste such that it is
the first penetration measurement that does not mark the specimen surface with a complete
circular impression
Molding Test Specimen—Quickly form the cement paste, into a ball with gloved hands and toss
six times from one hand to the other, maintaining the hands about 150 mm (6 in.) apart. Press the
ball, resting in the palm of the hand, into the larger end of the conical ring, G, held in the other
hand, completely filling the ring with paste. Remove the excess at the larger end by a single
movement of the palm of the hand. Place the ring on its larger end onto the non-absorptive
plate, H, and slice off the excess paste at the smaller end at the top of the ring by a single oblique
stroke of the trowel held at a slight angle with the top of the ring. Smooth the top of the
specimen, if necessary, with one or two light touches of the pointed end of the trowel.
During the operation of cutting and smoothing, take care not to compress the paste. Immediately
after molding, place the test specimen in the moist cabinet or moist room and allow it to remain
there except when penetration measurements are being made. The specimen shall remain in the
conical mold, supported by the non-absorptive plate throughout the test period.
Time of Setting Determination—Allow the time of setting specimen to remain in the moist
cabinet or moist room for 30 min after molding without being disturbed. Determine the
penetration of the 1-mm needle at this time and every 15 min thereafter (every 10 min for Type
III cements) until a penetration of 25 mm or less is obtained. Perform the penetration test by
lowering the needle D of the rod B until it rests on the surface of the cement paste. Tighten the
setscrew, E, and set the indicator, F, at the upper end of the scale, or take an initial reading.
Release the rod quickly by releasing the set screw, E, and allow the needle to settle for 30 s; then
take the reading to determine the penetration. At the option of the tester, if the paste is obviously
quite soft on the early readings, retard the fall of the rod to avoid bending the 1-mm needle, but
when actual penetration measurements to determine the time of setting are made, release the rod
only by the setscrew. Make each penetration test at least 5 mm away from any previous
penetration and at least 10 mm away from the inner side of the mold.
Record the results of all penetration tests and, by interpolation, determine the time when a
penetration of 25 mm is obtained. The elapsed time between the initial contact of cement and
water and the penetration of 25 mm is the VICAT time of setting or VICAT initial time of
setting.
Determine the VICAT final time of setting end point to be the first penetration measurement
that does not mark the specimen surface with a complete circular impression. Verify final set by
performing two additional penetration measurements on different areas of the specimen surface.
Obtain verification measurements within 90 s of the first “final set” measurement. The elapsed
time between the initial contact of cement and water and the end point determination above is the
VICAT final time of setting.
Precautions:
Fresh hydraulic cementitious mixtures are caustic and may cause chemical burns to skin
and tissue upon prolonged exposure. The use of gloves, protective clothing, and eye
protection is recommended.
Wash contact area with copious amounts of water after contact. Wash eyes for a
minimum of 15 min.
Avoid exposure of the body to clothing saturated with the liquid phase of the unhardened
material. Remove contaminated clothing immediately after exposure
The apparatus should be free from vibrations during all the test.
Making and curing
concrete test specimens
in the Field
ASTM Designation: C 31/C 31M
PRESENTATION OUTCOMES
• Why do we make these specimens?
• To know purpose of test conducted.
• To enable you to Make, cure and transport concrete test specimens under
field conditions.
Why do we make these specimens?
• Acceptance testing for specified strength.
• Checking adequacy of mixture proportions for specified strength
• Quality control.
Purposes the tests are conducted for
• Determination of whether a structure is capable of being put in service.
• Comparison with test results of standard cured specimens
• Adequacy of curing and protection
Making specimen
Apparatus:
• Cylinder mold (C 470)
• Beam mold (c 470)
• Tamping rod
• Internal vibrator (150 Hz)
• Mallet (o.6 kg)
• Sampling receptacle
• Slump apparatus (C 143)
• Air content apparatus (C 173)
• Temperature measuring device (C 1064)
Apparatus:
Slump test
• To check the adequacy of our concrete
• To decide the method of consolidation
• According to (ASTM C 143)
MOLDING
• • Place of molding should be; Flat, Rigid, Free from vibration, as near as
possible to storing place.
• Consolidation; Rodding and vibration
Rodding
Vibration
• Vibrator should be withdrawn slowly to avoid large air pockets
• Tap the sides of mold with mallet 10 to 15 times to eliminate the air
entrapped
Finishing
• Strike off extra concrete from the surface with least manipulation
• Level the surface with suitable tool like trowel or float.
• No projection or depression greater than 3.3 mm be tolerated.
• If desired, cap the surface of freshly made cylinder with a thin layer of
Portland cement paste.
Curing storage
• Move to a place where initial curing is possible immediately after finishing.
• Storing surface shall be levelled within 1⁄4 in. per feet [20 mm per m].
• Support the bottom of mold with flat surface during movement.
• Refinish the surface immediately if marred.
Curing continues… initial curing
• Initial curing temperature must be 16 to 27 °C during 1st 48 hours.
• Prevent moisture loss.
• Specific temperature(20-26 °C) needed for specific strength(40 MPa)
Curing continues… final curing
• Maintain water on the surface of specimen at all times.
• Keep temperature around 23 °C
• According to ASTM C 511
Beams
Beams are to be cured the same as cylinders except that they shall be stored in
water saturated with calcium hydroxide at [23 °C] at least 20 h prior to testing
Transportation
• Specimens shall not be transported until at least 8 h after final set.
• Prevent jarring damage
• Prevent freezing and over heating by proper insulation.
• Prevent moisture loss by wrapping specimen with plastic, burlaps etc.
• Transportation time shall not exceed 4 hours.
Report
• Report the following information to the laboratory that will test the
specimens:
1. Identification number.
2. Location of concrete represented by the samples.
3. Date, time and name of individual molding specimens.
4. Slump, air content, and concrete temperature, test results.
5. Curing method.
CE 3102 Course Outline
- Used to test the mechanical properties (tension, compression etc.) of a given test
specimen by exerting tensile, compressive or transverse stresses.
- The machine has been named so because of the wide range of tests it can perform over
different kind of materials. Different tests like peel test, flexural test, tension test, bend
test, friction test, spring test etc. can be performed with the help of UTM.
I. Loading Unit
1. Load Frame
The load frame of a universal testing machine can be made either by single support or by double
support. The load Frame consists of a table (where the specimen is placed for the compression
test), upper crosshead, and lower crosshead.
2. Upper Crosshead and Lower Crosshead
The upper crosshead is used to clamp one end of the test specimen. The lower crosshead in the
load frame is the movable crosshead whose screws can be loosened for height adjustment and
tightened. Both the crossheads have a tapered slot at the centre. This slot has a pair of racked
jaws that is intended to grip and hold the tensile test specimen.
3. Elongation Scale
The relative movement of the lower and upper table is measured by an elongation scale which is
provided along with the loading unit.
The main components of the control unit in a universal testing machine are:
This unit has a pendulum dynamometer unit that has a small cylinder with a piston which moves
with the non-pulsating oil flow. The pendulum is connected to the piston by pivot lever. The
pivot lever deflects based on the load applied to the specimen. This deflection is converted to the
load pointer and displays as the load on the dial.
The range of load application can be adjusted by means of a knob in the load measuring unit (0-
100 kN; 0-250 kN; 0-500 kN and 0-1000 kN). The accuracy of measuring unit controls the
overall accuracy of the machine.
3. Control Devices
The control devices can be electric or hydraulic. Electric control devices make use of switches to
move the crossheads and switch on/off the unit. A hydraulic control device consists of two
valves, Right Control Valve and Left Control Valve or Release Valve. A right control valve is
used to apply load on the specimen. The left control valve is used to release the load application
as shown in figure-1.
1. Tensile Test
2. Compression Test
3. Adhesion Tests
4. Pull-Out Tests
5. Bending Test
6. Hysteresis Test
UTM can be used to test a wide variety of materials like concrete, steel, cables, springs, steel
wires and chains, slings, links, rope, winches, steel ropes, etc.
UTM provides the value of load application and the respective displacements. From the observed
value, the load deflection graph is obtained. With the load value in the Y-axis and the
displacement in the X-axis. The displacement is actually the movement of the crossheads during
the load application.
From the load deflection graph, the stress-strain analysis, modulus of elasticity, yield strength of
the specimen tested can be determined.
WOOD
Wood, because of its availability, relatively low cost, ease of use, and durability (if properly
designed), continues to be an important civil engineering material. Wood is used extensively for
buildings, bridges, utility poles, floors, roofs, trusses, and piles. (See Figures 10.1 and 10.2.) Civil
engineering applications include both natural wood and engineered wood products, such as
laminates, plywood, and strand board.
In order to use wood efficiently, it is important to understand its basic properties and
limitations. In the United States, the Forest Service of the Department of Agriculture has broad
management responsibility for the harvesting of wood from public lands and for assisting private
sources with the selection of products for harvesting. This agency has produced the Wood
Handbook, which is an excellent document describing the characteristics and properties of wood
(USDA-FS, 1999).
This chapter covers the properties and characteristics of wood. In the design of a wood
structure, joints and connections often limit the design elements. These are generally covered in
a design class for wood construction and, therefore, are not considered in this text.
Wood is a natural, renewable product from trees. Biologically, a tree is a woody plant that
attains a height of at least 6 m (20 ft), normally has a single self-supporting trunk with no
branches for about 1.5 m (4 ft) above the ground, and has a definite crown. There are over 600
species of trees in the United States.
Trees are classified as either endogenous or exogenous, based on the type of growth.
Endogenous trees, such as palm trees, grow with intertwined fibers. Wood from endogenous
trees is not generally used for engineering applications in the United States. Exogenous trees
grow from the center out by adding concentric layers of wood around the central core. This book
considers only exogenous trees.
Exogenous trees are broadly classified as deciduous and conifers, producing hardwoods
and softwoods, respectively. The terms hardwood and softwood are classifications within the tree
family, not a description of the woods’ characteristics. In general, softwoods are softer, less
dense, and easier to cut than hardwoods. However, exceptions exist such as balsa, a very soft
and lightweight wood that is botanically a hardwood.
Deciduous trees generally shed their leaves at the end of each growing season.
Commercial hardwood production in the U.S. comes from 40 different tree species. Many
hardwoods are used for furniture and decorative veneers, due to their pleasing grain pattern. The
decorative properties of some hardwoods increase their value and cost. This makes them
uneconomical for construction lumber. Again, there are some exceptions where some hardwoods
are used engineered wood products that are used in construction applications.
Conifers, also known as evergreens, have needlelike leaves and normally do not shed
them at the end of the growing season. Conifers grow continuously through the crown, producing
a uniform stem and homogenous characteristics (Panshin & De Zeeuw, 1980). Softwood
production in the U.S. comes from about 20 individual species of conifers. Conifers are widely
used for construction. Conifers grow in large stands, permitting economical harvesting. They
mature rapidly, making them a renewable resource. Table 10.1 shows examples of hardwood and
softwood species (USDA-FS, 1999).
Structure of Wood
Wood has a distinct structure that affects its use as a construction material. Civil and
construction engineers need to understand the way the tree grows and the anisotropic nature of
wood in order to properly design and construct wood structures.
Chemical Composition
Lignin accounts for 23% to 33% of softwood and 16% to 25% of hardwood by weight.
Lignin is mostly an intercellular material. Chemically, lignin is an intractable, insoluble, material
that is loosely bonded to the cellulose. Lignin is basically the glue that holds the tubular cells
together. The longitudinal shear strength of wood is limited by the strength of the lignin bounds.
Hemicelluloses are polymeric units made from sugar molecules. Hemicellulose is different
from cellulose in that it has several sugars tied up in its cellular structure. Hardwood contains
20% to 30% hemicellulose and softwood averages 15% to 20%. The main sugar units in
hardwood and softwood are xylose and monnose, respectively.
The extractives compose 5% to 30% of the wood substance. Included in this group are
tannins and other polyphenolics, coloring matters, essential oils, fats, resins, waxes, gums,
starches, and simple metabolic intermediates. These materials can be removed with simple inert
neutral solvents, such as water, alcohol, acetone, and benzene. The amount contained in an
individual tree depends on the species, growth conditions, and time of year the tree is harvested.
The ash-forming materials account for 0.1% to 3.0% of the wood material and include
calcium, potassium, phosphate, and silica.
Moisture Content
The moisture content of a wood specimen is the weight of water in the specimen
expressed as a percentage of the oven-dry weight of the wood. An oven-dried wood sample is a
sample that has been dried in an oven at 100°C to 105°C (212°F to 220°F) until the wood attains
a constant weight. Physical properties such as weight, shrinkage, and strength depend on the
moisture content of wood (Panshin & De Zeeuw, 1980).
Moisture exists in wood as either bound or free water. Bound water is held within the cell
wall by adsorption forces, whereas free water exists as either condensed water or water vapor in
the cell cavities. In green wood, the cell walls are saturated. However, the cell cavities may or
may not contain free water. The level of saturation at which the cell walls are completely
saturated, but no free water exists in the cell cavities, is called the fiber saturation point (FSP).
FSP varies from species to species and within the same species, but is typically in the range of
21% to 32%. The FSP is of great practical significance, because the addition or removal of
moisture below the FSP has a large effect on practically all physical and mechanical properties of
wood, whereas above the FSP, the properties are independent of moisture content.
When the moisture content of wood is above the fiber saturation point, the wood is
dimensionally stable. However, moisture fluctuations below the FSP always result in dimensional
changes. Shrinkage is caused by loss of moisture from the cell walls, and conversely, swelling is
caused by the gain of moisture in the cell walls. Figure 10.5 shows that the changes in wood
dimensions vary from one direction to another. Dimensional changes in the radial direction are
generally one-half the change in the tangential direction. Swelling and shrinkage in the
longitudinal direction is minimal, typically 0.1% to 0.2% for a change in the moisture content
from the FSP to oven dry. This anisotropy of dimensional changes of wood causes warping,
checking, splitting, and structural performance problems, as discussed in more detail later in the
chapter. It is also the reason that the sawing pattern of boards affects the amount of distortion
when subjected to changes in moisture.
For engineering calculations, the FSP is commonly assumed to be 30%. This is easier to
remember and more useful than expecting the engineer to find and use species-specific values.
The same applies for shrinkage calculations. Tangential shrinkage can be assumed to be 8% and
radial shrinkage 4%. For structural lumber where growth ring or orientation is not known in
advance and can be reasonably expected to vary from piece to piece, a value of 6% is commonly
chosen for shrinkage from a FSP (30%) to oven-dry (0%). Thus, shrinkage could be estimated
as 6% shrinkage in 30% change in moisture content, or 1% shrinkage per 5% change in moisture
content. This is the rule of thumb recommended by the American Institute of Timber Construction
(AITC) for calculating shrinkage of a glue laminated (glulam) beam, which consists of several
laminations of varying growth ring orientations.
The moisture content in wood varies depending on air temperature and humidity.
However, the natural change of moisture content is a slow process, so as atmospheric conditions
change, the moisture content in wood tends to adjust to conditions near the average. The
moisture content for the average atmospheric conditions is the equilibrium moisture content
(EMC). The wood handbook includes values of the EMC as a function of temperature and humidity.
The EMC ranges from less than 1%, at temperatures greater than 55°C (130°F) and 5% humidity,
to over 20% at temperatures less than 27°C (80°F) and 90% humidity.
Strength properties of wood vary to a large extent, depending on the orientation of grain
relative to the direction of force. For example, the tensile strength in the longitudinal direction
(parallel to grain) is more than 20 times the tensile strength in the radial direction (perpendicular
to grain). Also, tensile strength parallel to grain is larger than the compressive strength in the
same direction for small, clear specimens. In full size structural members, the tensile strength
controls the capacity of most pieces. Also, tension is more sensitive to strength-reducing
characteristics such as knots and slope of grain. Common strength properties for wood include
modulus of rupture in bending, compressive strength parallel and perpendicular to the grain,
tensile strength parallel to the grain, and shear strength parallel to the grain. Some of the less
common strength properties are torsion, toughness, and fatigue strength.
Load Duration
Wood can support higher loads of short duration than sustained loads. Under sustained
loads, wood continues to deform. The design values of material properties contemplate fully
stressing the member to the tabulated design values for a period of 10 years and/or the
application of 90% of the full maximum load continuously throughout the life of the structure. If
the maximum stress levels are exceeded, the structure can deform prematurely.
Generally, a load duration of 10 years is used for design. Typical load duration factors that
would be applied to the values in Tables 10.3 and 10.4 (except for compression perpendicular to
the grain) are shown in Figure 10.13. For example, if a floor joint is designed for a temporary
stage that is used only for a one-day presentation, the allowable bending fiber stress can be
increased by 33 percent over the allowable stress for a normal application.
F I G U R E 1 0 . 1 3 Adjustment factors for load duration working-stress for wood design
based on 10-year nominal duration. Reprinted with permission of American Forest and Paper
Association (1997).
Standard mechanical testing methods for wood are designed almost exclusively to obtain
data for predicting performance. To achieve reproducibility in the testing environment,
specifications include methods of material selection and preparation, testing equipment and
techniques, and computational methods for data reduction. Standards for testing wood and wood
composites are published by ASTM, the U.S. Department of Commerce, the National Standard
Institute (NSI), and various other trade associations, such as the Western Woods Product
Association.
Due to the many variables affecting the test results, it is of primary importance to correctly
select the specimen and type of test. There are two main testing techniques for establishing
strength parameters: the testing of timbers of structural sizes and the testing of representative,
small, clear specimens.
Testing of structural-size timbers provides relationships among mechanical and physical
properties, working stress data, correlations between environmental conditions, wood
imperfections, and mechanical properties. The primary purposes for testing small, clear
specimens are to obtain the mechanical properties of various species and to provide a means of
control and comparison in production activities. Testing of structural-size members is more
important than testing small, clear specimens since the design values are more applicable to the
actual size members. ASTM D198 presents the testing standards for full-size tests, whereas ASTM
D143 presents the testing standards for small, clear wood specimens.
Figure 10.14 shows a schematic of test specimens of wood tested in tension, compression,
bending, and hardness.
For both full-size lumber and small, clear specimens, the bending test is more commonly
used than the other tests.
F I G U R E 1 0 . 1 4 Test specimens of wood: (a) tension parallel to grain, (b) tension
perpendicular to grain, (c) compression parallel to grain, (d) compression perpendicular to
grain, (e) hardness perpendicular to grain, (f) hardness parallel to grain, and (g) bending. (©
Pearson Education, Inc. Used by permission.)
The flexure test is performed on members in sizes that are usually used in structural
applications. The test specimen may be solid wood such as laminated wood, or a composite
construction of wood or of wood combined with plastics or metals. The test method is intended
primarily for beams of rectangular cross section, but is also applicable to beams of round and
irregular shapes, such as round posts, I-beams, or other special sections. The member is
supported near its ends and is subjected to two-point, third-point, or center-point loading as
shown in Figure 10.15, depending on the purpose of the test. Figure 10.16 illustrates a two-point
loading flexure test on a glulam structural member.
The span of the beam varies depending on the member size. Specimens with a depth-to-
width ratio of three or greater require lateral support to avoid instability. Loading is continued
until complete failure or an arbitrary terminal load has been reached. The load and the deflection
of the neutral axis of the beam at the center of the span are recorded during the test. From the
load-deflection data, the following data are noted: load and deflection at first failure, at maximum
load, and at points of sudden change. Properties that can be obtained from the test include fiber
stress at proportional limit, modulus of rupture, modulus ofelasticity, and maximum shear stress.
The results of this test can be used in several applications, such as the development of grading
rules and specifications, development of working stresses, and checking the influence of
imperfections on the mechanical properties of structural members.
Design Considerations
Measurement of wood properties in the lab does not reflect all the factors which affect
behaviour of the material in engineering applications. For design of wood structures, the strength
properties given in Tables 10.3 and 10.4 must be adjusted for the following (National Design
Specification® for Wood Construction, 2005):
8
MASONRY
Width
Length Height
FIGURE 8.2 Examples of masonry units: (a) concrete masonry units, (b) clay
bricks, and (c) structural clay tiles.
Maximum Water
Weight Unit Weight Absorption kg/m3 1lb/ft32
Classification Mg/m3 1lb/ft32 (Average of 3 units)
cinders, expanded clay, and expanded shale are used to manufacture lightweight
units. Lightweight units have higher thermal and fire resistance properties and lower
sound resistance than normal weight units.
Concrete masonry units are manufactured using a relatively dry (zero-slump)
concrete mixture consisting of portland cement, aggregates, water, and admixtures.
Type I cement is usually used to manufacture concrete masonry units; however,
Type III is sometimes used to reduce the curing time. Air-entrained concrete is
sometimes used to increase the resistance of the masonry structure to freeze and
thaw effects and to improve workability, compaction, and molding characteristics of
the units during manufacturing. The units are molded under pressure, then cured,
usually using low-pressure steam curing. After manufacturing, the units are stored
under controlled conditions so that the concrete continues curing.
Concrete masonry units can be classified as load bearing (ASTM C90) and
non–load bearing (ASTM C129). Load-bearing units must satisfy a higher minimum
compressive strength requirement than non–load-bearing units, as shown in Table 8.2.
The compressive strength of individual concrete masonry units is determined by
capping the unit and applying load in the direction of the height of the unit until
failure (ASTM C140). A full-size unit is recommended for testing, although a portion of
a unit can be used if the capacity of the testing machine is not large enough. The gross
area compressive strength is calculated by dividing the load at failure by the gross
cross-sectional area of the unit. The net area compressive strength is calculated by
dividing the load at failure by the net cross-sectional area. The net cross-sectional area
is calculated by dividing the net volume of the unit by its average height. The net
volume is determined using the water displacement method according to ASTM C140.
Solution
a. Gross area = 7.625 * 15.625 = 119.141 in3
Gross area compressive strength = 250,000/119.141 = 2,098.4 psi
b. Net area = 366.9/7.625 = 48.118 in2
Net area compressive strength = 250,000/48.118 = 5,195.6 psi
Ws - Wd
Absorption 1kg/m32 = * 1000 (8.1)
Ws - Wi
Ws - Wd
Absorption 1lb/ft32 = * 62.4 (8.2)
Ws - Wi
Ws - Wd
Absorption 1%2 = * 100 (8.3)
Wd
Wr - Wd
Moisture content as a percent of total absorption = * 100 (8.4)
Ws - Wd
Section 8.1 Masonry Units 319
where
Ws = saturated weight of specimen, kg (lb)
Wd = oven-dry weight of unit, kg (lb),
Wi = immersed weight of specimen, kg (lb), and
Wr = weight of specimen as received
Table 8.1 shows the allowable maximum water absorption for load-bearing
concrete masonry units.
A concrete masonry unit was tested according to ASTM C140 procedure and produced
the following results:
Calculate the absorption in kg/m3, percent absorption, and moisture content of the unit
as a percent of total absorption.
Solution
11,089 - 9,893
Absorption = * 1000 = 200.1 kg/m3
11,089 - 5,136
11,089 - 9,893
Percent absorption = * 100 = 12.1%
9,893
Moisture content as a percent of total absorption
10,354 - 9,893
= * 100 = 38.5%
11,089 - 9,893
Concrete masonry units are available in different sizes, colors, shapes, and
textures. Concrete masonry units are specified by their nominal dimensions.
The nominal dimension is greater than its specified (or modular) dimension by
the thickness of the mortar joint, usually 10 mm (3/8 in.). For example, a
200 mm * 200 mm * 400 mm 18 in. * 8 in. * 16 in.2 block has an actual width
of 190 mm (7-5/8 in.), height of 190 mm (7-5/8 in.), and length of 390 mm (15-5/8
in.), as illustrated in Figure 8.3. Load-bearing concrete masonry units are avail-
able in nominal widths of 100 mm, 150 mm, 200 mm, 250 mm, and 300 mm (4 in.,
6 in., 8 in., 10 in., and 12 in.), heights of 100 mm and 200 mm (4 in. and 8 in.), and
lengths of 300 mm, 400 mm, and 600 mm (12 in., 16 in., and 24 in.). Also,
320 Chapter 8 Masonry
depending on the position within the masonry wall, they are manufactured as
stretcher, single-corner, and double-corner units, as depicted in Figure 8.4.
Solid concrete masonry units (concrete bricks) are manufactured in two types
based on their exposure properties: concrete building bricks (ASTM C55) and con-
crete facing bricks (ASTM C1634). The concrete building bricks are manufactured for
general use in non-facing, utilitarian applications, while the concrete facing bricks are
typically used in applications where one or more faces of the unit is intended to be
exposed. The concrete facing bricks have stricter requirements than the concrete
building bricks. The maximum allowable water absorption of the concrete facing
bricks is less than that of the concrete building bricks. Also, the minimum net area
compressive strength of the concrete facing bricks is higher than that of the concrete
building bricks as shown in Table 8.3.
These walls are constructed from the foundation level and post-tensioning rods
are anchored into the foundation. These rods are run vertically between the
wythes or in the core of concrete masonry units.
After the masonry wall construction is completed and cured, these rods are
tensioned and anchored on the steel place at the top of the wall.
CE 3102A PORTLAND CEMENT CONCRETE
HISTORY
The development of cementing materials can be traced back to the Egyptians and Romans
and their use of masonry construction.
The Egyptians used cement produced by heating process, and this may have been
the start of the technology.
Roman engineering upgraded simple lime mortars with the addition of volcanic ash
which increased their durability, as evidenced by the sound structures that still stand.
A good example of the durability and longevity of Roman concrete is the Aqua Virgo
built around 19 B.C. Today it still carries spring water over 11 miles to the Trevi
Fountain in Rome.
The development of concrete or cement technology as we know it today probably
can be traced back to England, wherein 1824 Joseph Aspdin produced a Portland
cement from a heated mixture of limestone and clay. He was awarded a British
patent, and the name “Portland cement” was used because when the material
hardened, it resembled a stone from the quarries of Portland, England.
The sources of these elements vary from one manufacturing location to another, but once
these materials are obtained, the process is rather uniform (Table 4–2).
For practical purposes, Type I Portland cement contains the oxides illustrated in Table 4–3.
Portland cements are composed of four basic chemical compounds, shown with their
names, chemical formulas, and abbreviations:
1. Tricalcium silicate
Tricalcium silicate hardens rapidly and is largely responsible for initial set and early
strength. In general, the early strength of Portland cement concretes will be higher
with increased percentages of [Link], if moist curing is continued, the later
strength after about 6 months will be greater for cements with a higher percentage of
C2S.
2. Dicalcium silicate
Dicalcium silicate hardens slowly, and its effect on strength increases occurs at ages
beyond one week.
3. Tricalcium aluminate
Tricalcium aluminate contributes to strength development in the first few days
because it is the first compound to hydrate.
It is, however, the least desirable component because of its high heat generation and
its reactiveness with soils and water containing moderate-to-high sulfate
concentrations.
Cements made with low C3A contents usually generate less heat, develop higher
strengths, and show greater resistance to sulfate attacks.
4. Tetracalcium aluminoferrite
Tetracalcium aluminoferrite assists in the manufacture of portland cement by
allowing lower clinkering temperature.
C4AFe contributes very little to the strength of concrete even though it hydrates very
rapidly.
1. One factor which affects the hydration of cement, regardless of its chemical
composition, is its fineness.
The finer a cement is ground, the higher the heat of hydration and resulting
accelerated strength gain. The strength gain due to fineness is evident during
the first 7 days.
Currently the fineness of cement is stated as specific surface (i.e., the
calculated surface area of the particles in square meters per kilogram [m2/kg]
of cement).
Even though the specific surface is only an approximation of the true area,
good correlations have been obtained between specific surfaces and those
properties influenced by particle fineness. Higher specific surfaces indicate a
finer-ground, and usually a more active, cement.
2. Soundness
is the ability of a cement to maintain a stable volume after setting.
Unsound cement will exhibit cracking, disruption, and eventual disintegration
of the material mass. This delayed-destruction expansion is caused by
excessive amounts of free lime or magnesium.
The free lime is enclosed in cement particles, and eventually the moisture
reaches the lime after the cement has set.
At that time the lime expands with considerable force, disrupting the set
cement. The current test for soundness in cement is the ASTM Autoclave
test. Standard specimens of neat cement paste are subjected to high
pressure and temperature for 3 hours. After cooling, the length of bars is
compared with the length before testing and cements that exhibit an
expansion of no more than 0.50 percent are considered to be sound. Since
the introduction of the Autoclave test, there have been almost no cases of
delayed expansion due to unsound cements.
Portland-Pozzolan Cements
IP, IP-A, P, and P-A designate the portland-pozzolan cements with the A denoting air-
entraining additives as specified in C595. They are used principally for large hydraulic
structures such as bridge piers and dams. These cements are manufactured by
intergrinding Portland cement clinker with a suitable pozzolan such as volcanic ash, fly ash
from power plants, or diatomaceous earth, or by blending the portland cement or portland
blast-furnace slag cement and a pozzolan.
Masonry Cements
Type I and Type II masonry cements are manufactured to conform to ASTM C91 and
contain Portland cement, air-entraining additives, and materials selected for their ability to
impart workability, plasticity, and water-retention properties to the masonry mortars.
6.7.1 Setting
Setting
- Refers to the stiffening of the cement paste or the change from a plastic state to a
solid state.
- Although with setting comes some strength, it should be distinguished from
hardening, which refers to the strength gain in a set cement paste.
- The term setting implies solidification of the plastic cement paste. Initial and final
setting times may be regarded as the two stiffening states of the cement.
Initial set and final set. The definitions of the initial and final sets are
arbitrary, based on measurements by either the Vicat apparatus (ASTM
C191) or the Gillmore needles (ASTM C266).
Initial set
- The beginning of solidification.
- Marks the point in time when the paste has become unworkable.
- The initial setting time may be defined as the time taken by the paste to stiffen to
such an extent that the Vicat’s needle is not permitted to move down through the
paste to within 5 ± 0.5 mm measured from the bottom of the mould.
Final set
- The time taken to solidify completely.
- This should not be too long in order to resume construction activity within a
reasonable time after the placement of concrete.
- The final setting time is the time after which the paste becomes so hard that the
angular attachment to the needle, under standard weight, fails to leave any mark on
the hardened concrete.
The initial set time must allow for handling and placing the concrete before
stiffening. The maximum final set time is specified and measured to ensure
normal hydration.
Due to the differences in the test apparatuses and procedures, the Vicat and Gillmore tests
produce different results for a single sample of material.
Setting time of cement is rapid with the increase in the fineness of cement. When the mixing
water used in testing cement paste is increased by 1 per cent above that required for
normal consistency, an increase of about 30 minutes or more is observed in the initial or
final set.
Cements stored in warm rooms will, in general, be quick setting than those stored in cold
places. Cold mixing water retards set while warm water accelerates it. Cement exposed to
thoroughly saturated atmosphere will set much more slowly than those exposed to a dry
atmosphere.
STEEL
Pig iron is further oxidized in another furnace at about 3000°F (1650°C) to produce steel.
Most steel is made by the basic oxygen process, electric-arc process, open-hearth process,
or vacuum process. Each has unique features, but in all cases, pig iron, scrap steel, and
sometimes iron ore are melted together with a flux of limestone or lime. The process is a
repetition of the blast-furnace operation with variations. The purpose is the same—to
remove impurities. Impurities are removed as gases and in the slag.
Phosphorus and sulfur are reduced to less than 0.05 percent of the steel. Manganese
content is reduced to an amount from 0.2 to 2.0 percent; silicon from 0.01 to 0.35 percent.
The final amounts depend on the specifications for the steel. Carbon is the key element in
controlling the properties of ordinary steel called carbon steel. Strength and hardness
increase with an increase in carbon up to about 1.2 percent. Brittleness increases and
ductility decreases as carbon increases. Usually an amount less than 1.2 percent is
specified in order to obtain a product satisfactory in all respects.
Steel is defined as a chemical union of iron and carbon (carbon is, therefore, less than 2
percent by weight) plus other elements. This definition does not exclude every kind of iron.
However, almost all kinds of iron contain carbon in excess of 2 percent and steel usually
contains less than 1.2 percent carbon. Therefore, it is usually obvious whether a ferrous
metal is iron or steel. Customary terminology should be used for borderline cases. The term
iron is used to refer to cast iron, malleable cast iron, ductile iron, wrought iron, or pure iron.
As can be seen in Table 5–2, some of these metals may have less than 2 percent carbon.
Carbon, manganese, silicon, phosphorus, and sulfur are considered impurities because
generally they must all bereduced below the amount found in iron ore. However, when
present in the correct amount, each of these elements improves the final product. In some
cases, due to the characteristics of the iron ore, there is a deficiency of one or more of these
elements, and they must be added to the molten steel.
Any added element is considered an alloying element, but when only the
aforementioned five elements are involved, the steel is not considered an alloy steel. Other
elements may be added to impart certain properties to steel. These are also called alloying
elements, and the steel that results is called alloy steel. Table 5–3 shows the effects of
alloying elements.
Steels are identified according to a classification system of the Society of Automotive
Engineers (SAE). Each type of steel is designated by a group of numbers. The first digit
indicates the class of steel. For example, carbon steel is designated by No. 1 and nickel
steel by No. 2. The next one or two digits indicate the approximate percentage of the major
alloying element for alloy steels. The last two or three digits indicate the carbon content in
hundredths of a percent. The classification system is outlined in Table 5–4.
Besides the key information shown directly by the classification number, percentage
ranges for all impurities and alloying elements are also designated indirectly when the
system is used. The system provides a simplified way to specify steel. For example, a 1018
steel is a carbon steel containing 0.15 to 0.20 percent carbon, 0.60 to 0.90 percent
manganese, 0.040 maximum percent phosphorus, and 0.050 maximum percent sulfur; and
4320 steel is a molybdenum steel containing 0.17 to 0.22 percent carbon, 0.45 to 0.65
percent manganese, 0.040 percent phosphorus, 0.040 percent sulfur, 0.20 to 0.35 percent
silicon, 1.65 to 2 percent nickel, 0.40 to 0.60 percent chromium, and 0.20 to 0.30 percent
molybdenum.
The American Iron and Steel Institute has adopted the SAE system with some variations
and has added letter prefixes to designate the steel-making process used and other letters
to designate special conditions. These designations are also shown in Table 5–4. Table 5–5
shows the American Institute of Steel Construction, Inc. (AISC) system of designating
structural steel. Each steel is known by the number of the ASTM standard that describes it.
However, manufacturers may call them by trade names. The figure shows which rolled
plates, bars, and shapes are made of each type of steel. For example, it can be seen that
A529 Gr. 50 steel is carbon steel with a yield stress of 50 Ksi or more and ultimate tensile
stress of 65–100 Ksi, and that only shapes listed in group 1, table A of ASTM A6 and plates
and bars up to 1⁄2 in. thickness are manufactured. ASTM A529 specifies manufacturing
methods, chemical content, and mechanical properties required of steel to be supplied
when A529 steel is specified.
Steel properties are influenced to a great extent by the mechanical operations that
change an ingot of steel into a useful shape. The operations are rolling, extruding, drawing,
forging, and casting. All except casting may be performed while the steel is in a plastic
condition at a temperature of about 2000°F (1090°C), or as low as room temperature. The
operations are called hot working or cold working.
Hot working breaks up coarse grains and increases density by closing tiny air holes and
forcing the grains closer together. Cold working elongates grains in the direction of the steel
elongation, increases strength and hardness, and decreases ductility. Cold working results
in more accurately finished products, because there is no cooling shrinkage to be estimated.
The surfaces are smoother, because oxide scale does not form as it does during hot
working. Overworking, whether hot or cold, causes brittleness.
For all but very large objects, working to final shape is done in two stages. The first
stage consists of squeezing the ingot into a smaller cross section between two rollers,
called blooming rolls, which exert a very high pressure. This operation is always performed
while the steel is hot. In the second stage, the ingot is rolled into a much longer piece with a
square or rectangular cross section closer to its final size. The desired cross section is
obtained by turning the ingot 90° to be rolled on the sides as it is passed back and forth
through the rolls. If it is approximately square in cross section, it is called a bloom if large
(over 36 sq in.) and a billet if smaller. It is called a slab if the width is twice the thickness or
more. The appropriate shape is used to manufacture beams, rails, plate, sheets, wire, pipe,
bolts, or other items by one of the following methods.
Rolling consists of compressing and shaping an ingot into a useful shape by squeezing it
through a succession of rollers, each succeeding set of rollers squeezing the material
smaller in cross section and closer to the final shape. The piece being rolled becomes
longer and wider as it is compressed. It may be made narrower by cutting or by rolling after
turning 90° so that the rolling reduces the width. A wide variety of cross sections useful for
construction of buildings and bridges can be rolled in long pieces by means of specially
shaped rollers (Figure 5–5). Flat sheets can be rolled by rollers of a constant diameter.
Corrugated sheets can be rolled from flat sheets by using corrugated rollers. Corrugated
steel roof deck can be seen in Figure 5–15. Hot rolling usually precedes cold rolling until the
steel is close to its final shape. Hot rolling is usually the first step in reducing the size of an
ingot prior to extruding, drawing, or forging.
Extrusion consists of forcing a billet of hot, plastic steel through a die of the desired
shape to produce a continuous length of material of reduced cross section in the shape of
the die. The resulting product has the shape of a rolled product; that is, it is long with a
constant cross section. However, more intricate shapes can be formed by extrusion than by
rolling, and the surface is of higher quality. An extrusion is made in one operation rather
than repetitive operations as in the case of rolling. An extruded section can sometimes be
used in place of a section that requires several operations if formed any other way (Figure
5–6). Extrusions can be made with cross sections having a maximum dimension of nearly 2
ft.
Drawing consists of pulling steel through a small die to form wire or a small rod of round,
square, oval, or other cross section. Steel is hot rolled to form a rod of a size not much
larger than the shape to be drawn. It is then finished by cold drawing. Seamless steel pipe
may also be finished by cold drawing over a round, bullet-shaped mandrel to form a hollow
center and through a die to form the outside. The advantages of cold drawing are a
smoother finish, more accurate size, more strength, and better machinability.
Forging consists of deforming steel by pressure or blows into a desired shape. The
forging may be made from an ingot or from a rolled shape. The steel is usually heated to a
semisolid state at a temperature over 2000°F (1090°C). In some cases it is forged cold. It is
forced to fill the shape between dies by pressure or blows of the upper die upon the lower
one. The shape may be formed more accurately by successive forgings, each succeeding
operation performed with smaller dies closer to the desired final shape. Instead, the final
shape may be achieved by machining. Many shapes can be either cast or forged.
Economics often determine which method is used. However, forging is preferred if strength
of the part is important. Forging improves the mechanical properties of the metal, as does
other hot working or cold working, and produces a stronger, more ductile, more uniform
product with smaller grain size than is produced by casting.
After steel cools and is given its final shape, further heating and cooling processes can
change the internal structure and thereby impart certain properties. Heat treatment consists
of heating, holding the metal at the high temperature, and cooling. Even here the rate of
heating is not important, except for high-carbon alloyed steels. The metal is held at the
upper temperature so that it can be heated to a uniform temperature throughout. The rate of
cooling is very important.
Annealing consists of heating the steel to a temperature slightly lower than for
normalizing and cooling it several hundred degrees very slowly, usually in a furnace.
Methods vary somewhat depending on the purpose, which may be to soften the metal,
produce a special structure, facilitate machining and cold shaping, or reduce stresses.
Quenching consists of cooling steel very rapidly in oil, water, or brine from a temperature
of about 1500°F (815°C). Quenching increases hardness and strength, but reduces ductility
and toughness. Residual stresses are introduced by quenching and should be relieved by
tempering.
Mechanical tests for steel include tension, bending, hardness, and impact. For structural
steel the tension, or tensile, test is the most important (Figure 5–7). The purchaser may
specify that the test be performed on steel from the furnace, after rolling, or after fabrication.
Specimens for testing are poured separately as an ingot is being made or are cut from the
waste material of a rolled member. Specimens may be of various sizes.
Before the force is applied, two marks are made on the specimen 2 in. apart in the
direction of the applied force. The two marks are drawn farther apart as the specimen
deforms under the tension. Strain is calculated by dividing the increase in distance between
the marks by the original 2-in. distance.
Stress and strain are determined at regular intervals from readings of force and the
measured increase in distance between the marks. A curve of stress versus strain is plotted
to determine whatever information is desired. The yield stress and rupture stress are often
specified as lower limits for acceptance of steel. (Refer to Figure 1-3a for a typical
stress–strain diagram for steel.) In many cases, a complete stress–strain curve is plotted by
an automatic recorder as the test proceeds.
Automatic devices are available to determine yield strength by noting the strength at the
correct plastic (permanent) deformation as the sample is being tested without plotting a
stress–strain curve.
FIELD TEST OF
CONSTRUCTION MATERIALS
WHAT IS QUALITY ?
• Quality is usually defined as the ability of a
product or service to satisfy a given need.
• Hence quality is the Fitness for use.
Quality Assurance
vs. Quality Control
• Quality Assurance is
process oriented and
focuses on defect
prevention, while quality
control is product
oriented and focuses on
defect identification.
Quality Chain
Construction Materials
– Brick
– Concrete
– Stone
– Sand
– Cement
– Bitumen
– Steel
– GI sheet
– Electric wire
– Paint
Sampling
A sample is a limited quantity of something
which is intended to be similar to and represent
a larger amount of that thing
Test Frequency of Different
Construction Work contd.
Component Type/Name of Test Test Frequency
Bituminous i) Softening Point 1 per or part of 15000 sq.m
Material ii) Flash Point 1 per or part of 15000 sq.m
iii) Penetration 1 per or part of 7500 sq.m
iv) Gradation of FA 1 per or part of 7500 sq.m
v) Gradation of CA 1 per or part of 7500 sq.m
vi) Water absorption of CA 1 per or part of 7500 sq.m
vii) LAA 1 per or part of 7500 sq.m
viii) Flakiness Index 1 per or part of 7500 sq.m
Test Frequency of Different
Construction Work contd.
Component Type/Name of Test Test Frequency
Concrete i) FM of sand 1 per or part of 50 cu.m
ii) Water absorption of 1 per or part of 50 cu.m
coarse Aggregate
iii) LAA 1 per or part of 50 cu.m
iv) Gradation of Coarse 1 per or part of 50 cu.m
v) Aggregate 1 per or part of 50 cu.m
vi) Setting Time of Cement Set per or part of 75 cu.m
vii) Crushing Strength of Set per or part of 75 cu.m
Cement (3,7,28 days) Set per or part of 50 cu.m
viii) Crushing Strength of
Concrete
Test Frequency of Different
Construction Work contd.
Component Type/Name of Test Test Frequency
Brick Work i) Compressive Strength of Set per or part of 300 m3
Bricks
ii) Water Absorption of Set per or part of 300 m3
Bricks
iii) Efflorescence of Bricks Set per or part of 300 m3
iv) Setting time of cement Set per or part of 300 m3
v) Compressive Strength of Set per or part of 300 m3
Cement
vi) FM of Sand 1 per or part of 300 m3
Test Frequency of Different
Construction Work contd.
Component Type/Name of Test Test Frequency
Brick Work i) Compressive Strength of Set per or part of 300 m3
Bricks
ii) Water Absorption of Set per or part of 300 m3
Bricks
iii) Efflorescence of Bricks Set per or part of 300 m3
iv) Setting time of cement Set per or part of 300 m3
v) Compressive Strength of Set per or part of 300 m3
Cement
vi) FM of Sand 1 per or part of 300 m3