2. What is a composite?
◼ A material which is
composed of two or more
materials at a microscopic
scale and have physically /
chemically distinct phases.
◼ Examples:
Flesh in your leg reinforced
with bones
Concrete reinforced with steel
Epoxy reinforced with graphite
fibers.
3. ◼ Strictly speaking, the idea of
composite materials is not a
new or recent one.
◼ Nature is full of examples
wherein the idea of
composite materials is used.
◼ The coconut palm leaf, for
example, is essentially a
cantilever using the concept
of fiber reinforcement.
What is a composite?
4. Examples of Natural Composites
◼ Wood
Cellulose Fibers
Lignin Matrix
◼ Bones
Collagen Fibers
Mineral Matrix
Conditions of Composites :
1.Combination of materials should result in significant property changes
2. Content of the constituents is generally more than 10%
3. In general, property of one constituent is much greater (≥ 5) than the
other
5. Composites Demand
❖ Since the early 1960s, there has been an increasing demand for materials
that are stiffer and stronger yet lighter in fields as diverse as aerospace,
energy, and civil construction.
❖ It implies that, composite shall be used for the most efficient design of, say,
an aerospace structure, an automobile, a boat, or an electric motor,
6. Historical Perspective
◼ 4000 B.C. Fibrous composites were
used in Egypt in making laminated
writing materials
◼ 1939: Glass fiber manufactured
commercially for high temperature
electrical applications
◼ 1950s: Boron and carbon fibers were
produced to make ropes.
◼ 1960s: Matrix added to make
polymeric matrix composites
7. Historical Perspectives (continued)
◼ 1970s: Cold war forces development of metal
matrix composites for military aircrafts and
missile guidance systems
◼ 1990s: High temperature ceramic matrix
composites are being aggressively researched for
use in next generation aircraft engines and power
plant turbines
8. Advantages of composite
materials
◼ Lower density (20 to 40%)
◼ Higher directional mechanical properties (specific
tensile strength (ratio of material strength to density)
4 times greater than that of steel and aluminum.
◼ Higher Fatigue endurance .
◼ Higher toughness than ceramics and glasses.
◼ Versatility and tailoring by design.
◼ Easy to machine.??
◼ Can combine other properties (damping, corrosion).
◼ Cost.
9. Why composites over metals?
◼ High Strength and High
Stiffness
◼ Tailored Design
◼ Fatigue Life
◼ Dimensional Stability
◼ Corrosion Resistance
10. Why Composites over Metals?
◼ How is the mechanical advantage of
composite measured?
Strength
Ultimate
Density
Modulus
s
Young'
strength
Specific
modulus
Specific
=
=
=
ult
E
where
.
ult
=
,
E
=
13. Tailored Design
◼ Engineered to meet specific demands as
choices of making the material are many
more as compared to metals.
◼ Examples of choices
fiber volume fraction
layer orientation
type of layer
layer stacking sequence
14. Fatigue Life
◼ Fatigue life is higher than metals such as
aluminum.
◼ Important consideration in applications
such as
aircrafts
bridges
structures exposed to wind
15. Dimensional Stability
◼ Temperature changes can result
in overheating of components (example
engines)
thermal fatigue due to cyclic temperature
changes (space structures)
render structures inoperable (space antennas)
16. Corrosion Resistance
◼ Polymers and ceramics matrix are
corrosion resistant
◼ Examples include
underground storage tanks
doors
window frames
structural members of offshore drilling
platforms
18. Factors in Cost Estimate
◼ For Composite Materials
Fewer pounds are required
Fabrication cost may be lower
Transportation costs are generally
lower
Less maintenance than conventional
materials is required
20. Composites Classification
Based on Reinforced Materials
❖Fibre - a filament with L/D very high (of the order
1000)
❖A composite with fibre-reinforcement is called
Fibrous Composite
❖Particle – non fibrous with no long dimension
❖A composite with particles as reinforcement is
called Particulate Composite
❖Whiskers – nearly perfect single crystal fibre
❖Short, discontinuous, polygonal cross-section
22. Composites Classification
Polymer Matrix Composites (PMC)/ Carbon Matrix Composites
or Carbon-Carbon Composites
❖Polymers are structurally much more complex than metals or
ceramics. They are cheap and can be easily processed.
❖On the other hand, polymers have lower strength and modulus
and lower temperature use limits
❖ Polymers are generally poor conductors of heat and electricity.
Polymers, however are generally more resistant to chemicals than
are metals.
❖The process of forming large molecules from small ones is
called polymerization, that is, polymerization is the process of
joining many monomers
23. Composites Classification
❖Polymers that soften or melt on
heating are called thermoplastic
polymers and are suitable for
liquid flow forming
❖Examples include low- and
high-density polyethylene,
polystyrene, and polymethyl
methacrylate (PMMA).
❖When the structure is
amorphous, there is no apparent
order among the molecules and
the chains are arranged randomly;
Two main kinds of polymers are thermosets and
thermoplastics.
amorphous
24. Composites Classification
Two main kinds of polymers are thermosets and
thermoplastics.
semicrystalline
❖ When the molecules in a polymer are
crosslinked in the form of a network, they do
not soften on heating
❖We call such crosslinked polymers
thermosetting polymers. Thermosetting
polymers decompose on heating.
❖A typical example is that of rubber
crosslinked with sulfur, that is, vulcanized
rubber. Vulcanized rubber has ten times the
strength of natural rubber.
❖Common examples of thermosetting
polymers include epoxy, phenolic,
unsaturated polyester,
and vinyl ester.
25. Composites Classification
Metal Matrix Composites
❖ Metals are very versatile
engineering materials.
❖They are strong and tough. They
can be plastically deformed, and
they can be strengthened by a wide
variety of Methods
❖ mostly involving obstruction of
movement of lineal defects called
dislocations.
❖Most metals exist in one of the
following three crystalline forms:
❑ Face-centered cubic (fcc)
❑Body-centered cubic (bcc)
❑Hexagonal close packed (hcp).
26. Composites Classification
Metal Matrix Composites
Metals are crystalline materials; however, the crystalline structure is
never perfect. Metals contain a variety of crystal imperfections. We
can classify these as follows:
1. Point defects (zero dimensional),
2. Line defects (unidimensional),
3. Planar or interfacial defects (bidimensional), and
4. Volume defects (tridimensional).
28. Composites Classification
Why Fiber Reinforcement of Metals?
❖ Precipitation or dispersion hardening of a metal can result in
a dramatic increase in the yield stress and/or the work hardening
rate.
❖The influence of these obstacles on the elastic modulus is
negligible.
❖Their only function is to impede dislocation motion in the
metal.
❖The improvement in stiffness can be profitably obtained by
incorporating high modulus fibers in a metal matrix.
❖ It turns out that most of these high modulus fibers are also
lighter than the metallic matrix materials, the only exception
being tungsten, which has a high modulus and is very heavy.
29. Composites Classification
Ceramic Matrix Materials
❖The major disadvantage of ceramics is their extreme brittleness.
Even the minutest of surface flaws (scratches or nicks) or internal
flaws (inclusions, pores, or micro cracks) can have disastrous
results.
❖ One important approach to toughen ceramics involves fiber
reinforcement of brittle ceramics
Common Ceramic Matrix Materials
❖Silicon carbide has excellent high temperature resistance.
❖Silicon nitride is also an important nonoxide ceramic matrix
material.
❖Silica-based glasses and glass– ceramics are other ceramic matrices.
30. Composites Classification
Ceramic Matrix Materials
❖ Ceramic materials are very hard and brittle.
❖They have strong covalent and ionic bonds and very few slip
systems available compared to metals.
❖ High melting points, good corrosion resistance, stability at
elevated temperatures and high compressive strength.
❖ Naturally, ceramic matrices are the obvious choice for high
temperature applications.
❖High modulus of elasticity and low tensile strain, which most
ceramics posses, have combined to cause the failure of attempts to
add reinforcements to obtain strength improvement.
32. Advantages of Composites
◼ Specific Strength and Stiffness
◼ Tailored Design
◼ Fatigue Life
◼ Dimensional Stability
◼ Corrosion Resistance
◼ Cost-Effective Fabrication
33. Drawbacks of Composites
◼ High cost of fabrication of composites
◼ Complex mechanical characterization
◼ Complicated repair of composite structures
◼ High combination of all required properties
may not be available
34. Smart composites
❖ Composites containing shape memory alloys (SMA) as
an active component are a new class of advanced
structural and functional materials.
❖ They utilize the unique properties of SMA which change
their crystalline structure in response to the change of
temperature or stress.
❖ Depending on the temperature of deformation, the SMA
demonstrate two different types of mechanical behavior:
superelastic and pseudoplastic.
❖ In the superelastic regime it is possible to obtain almost
reversible deformations up to 10ˆ-1 with a very small
effective modulus which is many orders of magnitude
less than the elastic moduli of the parent material
35. Smart composites
❖ Superelasticity is also called “pseudoelasticity” and refers to the
condition when the functional temperature is above the austenite
finish temperature (Af)
❖ In this condition, NiTi is in the parent-structure austenite phase. By
applying stress, the phase transformation to the sheared derivative
structure/stress-induced martensite (SIM) will occur.
❖ In this situation the martensite phase is only stable in the presence
of stress and by removing the stress, martensite becomes
thermodynamically unstable, thus NiTi will reverse to the austenite
state and the original shape will be recovered.
36. Smart composites
❖ Therefore, in the case of superelasticity against the SME, no
thermal cycling is needed for transformation and large strains
applied by loading to SMAs can be recovered by unloading
37. Smart composites
❖ In the pseudoplastic regime the deformation proceeds
with small hardening up to very large strains but it is
irreversible.
❖ The residual strain can be removed by opposite loading
which recovers the microstructure to its initial state.
❖ The pseudoplastically deformed materials can be
completely recovered to their initial shape by heating.
❖ This is the so-called shape memory effect which gives its
name to this class of materials.
❖ Due to their special mechanical behavior, SMAs are
widely used in mechanical applications.
38. Smart composites
❖ There are examples of using them
as a component of functional and
structural composite
❖ Although they are in the stage of
research and development, these
materials have very good potential.
❖ One of the main obstacles for their
wider engineering applications is
the complex nonlinear behavior of
SMAs, strongly dependent on many
internal and external parameters.
❖ That is the reason why the
principles and characteristics of
SMAs are introduced first.
39. Smart Materials
❖ Smart materials are materials that are manipulated to
respond in a controllable and reversible way,
modifying some of their properties as a result of
external stimuli such as certain mechanical stress or a
certain temperature, among others.
❖ Because of their responsiveness, smart materials are also
known as responsive materials. These are usually
translated as "active" materials although it would be
more accurate to say "reactive" materials.
40. Smart Materials
❖ For example, we can talk about sportswear with
ventilation valves that react to temperature and
humidity by opening when the wearer breaks
out in a sweat and closing when the body cools down,
about drugs that are released into the bloodstream as
soon as a viral infection is detected.
41. Smart Materials
Piezoelectric materials
◼ They can convert mechanical energy into electrical
energy and vice versa. For example, they change their
shape in response to an electrical impulse or produce an
electrical charge in response to an applied mechanical
stress.
Shape memory materials
◼ They have the ability to change the shape, even
returning to their original shape, when exposed to a heat
source, among other stimuli.
42. Smart Materials
Chromoactive materials
◼ They change colour when subjected to a certain
variation in temperature, light, pressure, etc. Nowadays,
they are used in sectors such as optics, among others
Magnetorheological materials
◼ They change their properties when exposed to
a magnetic field. For example, they are currently used in
shock absorbers to prevent seismic vibrations in bridges
or skyscrapers.
◼ Photovoltaic materials or optoelectronics convert light
to electrical current.
43. Applications of Smart Materials
❖An “animated lamp” designed by
Romolo Stanco that uses shape-
memory alloy to change its shape
whenever it‟s turned on and off
❖Aircraft which will incorporate
"smart materials” that will allow
the wings of a craft to change
shape for optimal flying
conditions.
44. Interfaces
❖ The interface is the area where the different materials in
a composite coincide.
❖ In order to have a successful, applicable composite, one
must form an interface that is strong and favourable
towards maximum compatibility. A good interface is
imperative for a material to survive under stress.
45. Interfaces
❖ In viewing the above graphic of a fiber reinforced
matrix, one can see the presence of a medium that has
both the characteristics of the fiber and the matrix.
❖ The size of this gradient, the chemical interaction, and
the number of gradients present in a composite
determine the strength and application of the material.
❖ The same concept holds true for blends. The interphase
created between the components must achieve some
level of favourable interaction to prevent the materials
from "keeping to themselves" or phase separating.
❖ If phase separation occurs in a blend, then a
combination of properties is likely to be unsuccessful.
46. Interfaces
◼ The behaviour of a composite material is a result of the
combined behaviour of the following three entities:
• Fiber or the reinforcing element,
• Matrix, and
• Reinforcement/matrix interface.
47. Interfaces
◼ Wettability of the fiber or any other reinforcement by
the matrix and the type of bonding between the two
components constitute the primary considerations.
◼ It is important to appreciate the distinction between
wettability and bonding.
◼ One can have good wettability but weak bonding
between two components.
◼ On the other hand, one can also have strong bonding but
poor wettability, which in effect will mean weak
interface because we will have gaps or voids at the
interface because of the poor wettability.
49. Interfaces
Effect of Surface Roughness
◼ Generally, it is implicitly assumed that the substrate is
perfectly smooth. This, however, is far from true in
practice.
◼ More often than not, the interface between fiber and
matrix is rather rough instead of the ideal planar interface
50. Interfaces
❖ Characterization of surface roughness of a polycrystalline alumina
fiber (Nextel 610) by atomic force microscopy.
❖The three profiles on the left-hand side correspond to the two
horizonal and one vertical lines on the right-hand side figure.
❖The bottom figure shows a three-dimensional
perspective view of surface
51. Interfaces
Types of Bonding at the Interface
❖ It is important to be able to control the degree of
bonding between the matrix and the reinforcement.
❑ Mechanical bonding
❑Physical bonding
❑Chemical bonding
❑ Dissolution bonding
❑Reaction bonding.
52. Interfaces
Mechanical bonding
❖ Simple mechanical keying or interlocking effects
between two surfaces can lead to a considerable degree of
bonding.
❖In a fiber reinforced composite, any contraction of the
matrix onto a central fiber would result in a gripping of the
fiber by the matrix.
❖Imagine, for example, a situation in which the matrix in a
composite radially shrinks more than the fiber on cooling
from a high temperature.
❖This would lead to a gripping of the fiber by the matrix
even in the absence of any chemical bonding
53. Interfaces
Mechanical bonding
❖ Mechanical gripping due to
radial shrinkage of a matrix in a
composite on cooling from a
high temperature
❖ In general, mechanical
bonding is a low-energy bond,
i.e., the strength of a mechanical
bond is lower than that of a
chemical bond.
54. Interfaces
Mechanical bonding
(a) Good mechanical bond.
(b) Lack of wettability can make a liquid polymer or metal
unable to penetrate the asperities on the fiber surface,
leading to interfacial voids
55. Interfaces
Physical Bonding
❖Any bonding involving weak, secondary or van der
Waals forces, dipolar interactions and hydrogen
bonding can be classified as physical bonding.
❖ The bond energy in such physical bonding is very
low, approximately 8–16 kJ/mol.
56. Interfaces
Chemical Bonding
❖Atomic or molecular transport, by diffusional
processes, is involved in chemical bonding.
❖ Solid solution and compound formation may occur
at the interface, resulting in a reinforcement/matrix
interfacial reaction zone having a certain thickness.
This encompasses all types of covalent, ionic, and
metallic bonding.
❖ Chemical bonding involves primary forces and the
bond energy is in the range of approximately 40–400
kJ/mol.
57. Interfaces
Types of Chemical Bonding
❖ Dissolution bonding
❖ Reaction bonding
Dissolution bonding
❑ In this case, interaction between components occurs at an
electronic scale. Because these interactions are of rather short
range, it is important that the components come into intimate
contact on an atomic scale.
❑This implies that surfaces should be appropriately treated to
remove any impurities. Any contamination of fiber surfaces,
or entrapped air or gas bubbles at the interface, will hinder the
required intimate contact between the components.
58. Interfaces
Types of Chemical Bonding
❖ Dissolution bonding
❖ Reaction bonding
Reaction bonding
❑ In this case, a transport of molecules, atoms, or ions
occurs from one or both of the components to the
reaction site, that is, the interface.
❑This atomic transport is controlled by diffusional
processes. Such a bonding can exist at a variety of
interfaces, e.g., glass/polymer, metal/metal,
metal/ceramic, or ceramic/ceramic.