Composite Material Notes
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Transcript of Composite Material Notes
Unit 1 Introduction to Composite materials
Introduction
Modern technology required materials with unusual combination of properties that can’t
be met by conventional metal, alloys, ceramics, and polymeric materials. Composite is
the answer for structural materials that have low density, strong, stiff, abrasion, and
impact resistance and not easily corroded. In designing composite materials scientists and
engineers have indigenously combined various metals, ceramics and polymers to produce
a new generation of extra ordinary materials.
Definition
A composite material is defined as a structural material created by combining two or
more material having dissimilar characteristics. The constituent are combined at
macroscopic level and are not soluble in each other. One constituent is called Matrix
(Resin) phase and the other is called reinforcing (Fiber) phase. Reinforcing phase is
embedded in the matrix phase to give the desired characteristics.
Natural composite
Wood – lingix matrix reinforced with the cellulose fiber.
Bone – mineral matrix called apatite reinforced with collagen fibers.
Man made Composites
Mud walls of houses reinforced with bamboos
Glass fiber reinforced resin for helmet
Reinforced concrete
Automobile tyres
Need for developing composites
The main advantage of composite material is the combination of different
properties which are seldom found in conventional materials.
The unusual combination properties include high strength to weight ratio, higher
stiffness to weight ratio, improved fatigue resistance, improved corrosion
resistance, higher resistance to thermal expansion, excellent optical and magnetic
properties, wear resistance, good fracture toughness, acoustical insulation.
Present trend is to go for light weight construction for easy handling and reduced
space.
Classification of composites
1) Based on matrix
2) Based on Reinforcement
Reinforcements for the composites can be fibers, fabrics particles or whiskers. Fibers
are essentially characterized by one very long axis with other two axes either often
circular or near circular. Particles have no preferred orientation and so does their
shape. Whiskers have a preferred shape but are small both in diameter and length as
compared to fibers
Reinforcing material
ParticulateReinforced
FiberReinforced
Structural Reinforced
Functions of matrix
1) Binds the fiber together and acts as medium by which an externally applied stress
is transmitted and distributed to the fibers.
- matrix material should be ductile
- Elastic modulus of fiber should be much higher than that of matrix.
2) Matrix protects the individual fiber from surface damage as a result of mechanical
abrasion or chemical reaction with environment.
3) Matrix suppurates fibers and by the virtue of it relative softness and plasticity,
prevents the propagation of brittle cracks from fiber to fiber catastrophic failure.
In other word a matrix phase serves as a barrier to crack propagation.
Polymer Matrix Composites (PMC)
PMC’s consist of polymer resin as a matrix. They are used in greatest diversity of
composite applications as well as in largest quantity in light of there room temperature
properties, ease of fabrication and cost.
The matrix often determines the maximum service temperature, since it normally melts
softens and degrade as much as lower temperature then the fiber reinforcement.
Two main kinds of polymers are thermosets and thermoplastics. Thermosets have
qualities such as a well-bonded three-dimensional molecular structure after curing. They
decompose instead of melting on hardening. Merely changing the basic composition of
the resin is enough to alter the conditions suitably for curing and determine its other
characteristics. They can be retained in a partially cured condition too over prolonged
periods of time, rendering Thermosets very flexible. Thus, they are most suited as matrix
bases for advanced conditions fiber reinforced composites. Thermosets find wide ranging
applications in the chopped fiber composites form particularly when a premixed or
moulding compound with fibers of specific quality and aspect ratio happens to be starting
material as in epoxy, polymer and phenolic polyamide resins.
Thermoplastics have one- or two-dimensional molecular structure and they tend to at an
elevated temperature and show exaggerated melting point. Another advantage is that the
process of softening at elevated temperatures can reversed to regain its properties during
cooling, facilitating applications of conventional compress techniques to mould the
compounds.
Resins reinforced with thermoplastics now comprised an emerging group of composites.
The theme of most experiments in this area to improve the base properties of the resins
and extract the greatest functional advantages from them in new avenues, including
attempts to replace metals in die-casting processes. In crystalline thermoplastics, the
reinforcement affects the morphology to a considerable extent, prompting the
reinforcement to empower nucleation. Whenever crystalline or amorphous, these resins
possess the facility to alter their creep over an extensive range of temperature. But this
range includes the point at which the usage of resins is constrained, and the reinforcement
in such systems can increase the failure load as well as creep resistance.
Thermosets Thermoplastics
• Resin cost is low. • Resin cost is slightly higher.
• Thermosets exhibit moderate shrinkage. • Shrinkage of thermoplastics is
low
• Interlaminar fracture toughness is low. • Interlaminar fracture toughness
is high.
• Thermosets exhibit good resistance • Thermoplastics exhibit poor resistance
to fluids and solvents. to fluids and solvents.
• Composite mechanical properties are good. • Composite mechanical properties are good.
• Prepregability characteristics are excellent. • Prepregability characteristics are
poor.
• Prepreg shelf life and out time are poor. • Prepreg shelf life and out time are excellent.
Different types of thermosets and thermoplastic resins commonly in use are as follows:
Thermosets Thermoplastics
• Phenolics & Cyanate ester • Polypropylene
• Polyesters & Vinyl esters • Nylon (Polyamide)
• Polyimides • Poly-ether-imide (PEI)
• Epoxies • Poly-ether-sulphone (PES)
• Bismaleimide (BMI) • Poly-ether -ether-ketone (PEEK)
Metal Matrix Composite
Metal matrix composites, at present though generating a wide interest in research fraternity,
are not as widely in use as their plastic counterparts. High strength, fracture toughness and
stiffness are offered by metal matrices than those offered by their polymer counterparts. They
can withstand elevated temperature in corrosive environment than polymer composites. Most
metals and alloys could be used as matrices and they require reinforcement materials which
need to be stable over a range of temperature and non-reactive too. However the guiding
aspect for the choice depends essentially on the matrix material. Light metals form the matrix
for temperature application and the reinforcements in addition to the aforementioned reasons
are characterized by high moduli.
Most metals and alloys make good matrices. However, practically, the choices for low
temperature applications are not many. Only light metals are responsive, with their low
density proving an advantage. Titanium, Aluminum and magnesium are the popular matrix
metals currently in vogue, which are particularly useful for aircraft applications. If metallic
matrix materials have to offer high strength, they require high modulus reinforcements. The
strength-to-weight ratios of resulting composites can be higher than most alloys.
The melting point, physical and mechanical properties of the composite at various
temperatures determine the service temperature of composites. Most metals, ceramics and
compounds can be used with matrices of low melting point alloys. The choice of
reinforcements becomes more stunted with increase in the melting temperature of matrix
materials.
Ceramic Matrix Materials
Ceramics can be described as solid materials which exhibit very strong ionic bonding in
general and in few cases covalent bonding. High melting points, good corrosion resistance,
stability at elevated temperatures and high compressive strength, render ceramic-based
matrix materials a favorite for applications requiring a structural material that doesn’t give
way at temperatures above 1500ºC. 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. This is because at the stress levels at which ceramics rupture, there is
insufficient elongation of the matrix which keeps composite from transferring an effective
quantum of load to the reinforcement and the composite may fail unless the percentage of
fiber volume is high enough. A material is reinforcement to utilize the higher tensile strength
of the fiber, to produce an increase in load bearing capacity of the matrix. Addition of high-
strength fiber to a weaker ceramic has not always been successful and often the resultant
composite has proved to be weaker.
The use of reinforcement with high modulus of elasticity may take care of the problem to
some extent and presents pre-stressing of the fiber in the ceramic matrix is being increasingly
resorted to as an option.
When ceramics have a higher thermal expansion coefficient than reinforcement materials, the
resultant composite is unlikely to have a superior level of strength. In that case, the composite
will develop strength within ceramic at the time of cooling resulting in micro cracks
extending from fiber to fiber within the matrix. Micro cracking can result in a composite with
tensile strength lower than that of the matrix.
Reinforcement Types
Dispersoids –
Hard inert sub-micrometer size particles are disperse in to the metallic or non-metallic or
inter metallic matrix. More often particles of 0.01 micro-meter to 0.1 micro-meter are
uniformly dispersed in a value of concentration of 10 to 15%, which acts as obstacles for
dislocation movement. The presence of hard particle also increases the elastic limit causing
rapid hardening. The strength of composite depends up on the particle size, shape,
distribution and physical characteristics. In this composite material, matrix is the measure
load bearing constituent.
Particulate –
These types of composites consist of particles of one or more materials suspended in a matrix
of another material. Here size of particle varies from 1mm or more and volume concentration
varies from 20 to 40% volume. Because of slightly bigger size particle, they can’t interfere
with dislocation and exhibit strengthens effect by hydrostatically restraining the movement of
matrix close to it.
The elastic modulus of particulate composites follows the rule of mixture
Upper Limit Ec = Em Vm + Ep Vp
Lower Limit Ec= EmEp / (Em Vm + Ep Vp)
Ec, Ep, Em = Elastic modulus of composite, matrix and particulate
V = Volume fraction.
The rule of mixture equation predict that the elastic modulus should
Fiber Reinforcement
Fibers are grouped as whiskers, fibers and wires based diameter and character.
Whiskers – are vary thin single crystal, have extremely very large length to dia ratio (20 –
200). They have small size, high degree of crystalline perfection, high strength.
Ex – graphite, silicon, carbide, silicon nitride, Al oxide.
Fibers – Fiber materials are either polymer or ceramics which have small diameter.
Ex – polymer, glass, carbon, graphite, boron, silicon, quartz.
Wires – have relatively large diameter.
Ex – steel, tungsten, molybdenum.
* Discontinuous reinforcement -
Used in polymeric composite, referred as fillers of various shapes and short fibers up to
20 mm.
Ex – Metallic powders Al, Fe, Mg, Ti, Zr etc
Non metallic powder – Al oxides, calcium carbonate, silica, carbon etc
* Continuous fiber reinforcement -
Natural – Silk, Jute, Wool, Cotton
Organic – fibers from extended flexible polymers like polyethylene, polymer.
Glass fiber – Most inorganic fibers are based on amorphous 3D networks structure of
silica. They are isotropic in nature and can be drawn easily near their glass transition
temperature. Where they exhibit ‘Newtonian viscous flow’.
Depending on chemistry and property of fiber, they can be classified as
- E – glass – Electrical applications
- C – glass – Corrosion resistance application
- AR - Alkali resistance
- S – higher tensile and stiffness value
Structural Composites
a) Laminated
Multi layer composite consist several layers of fibrous composites bounded together by
organic adhesives. Each layer or lamina is a single layer composite and is very thin about
0.1 mm. when several such identical or different layers are bound together, form multi
layer composites. The constituent materials in each layer are called laminates. If multi
layer composite is made up of layers of different constituent materials. They are called
hybrid composites.
Ex – Reinforced plastic sheet clawed with copper, provided in the printed circuit which
gives better electrical conductivity.
Pure aluminum is bonded to high strength aluminum alloy protects ply from corrosion.
b) Sand witches
Sand witches consisting of thick low, density core, sand witched between two high
density facing materials. Sand witches can offer high strength and high bending stiffness.
Function of core – It suppurates the faces and resists deformation perpendicular to the
face plane.
It provides a certain degree of shear rigidity along planes which are perpendicular to the
face.
Core materials can be either sheets made of foam or honey comb structural made of
polystyrene foam, polyurethane foam, and polyvinyl chloride foam, plastic honey comb
carbon or Kevlar.
Face sheet is generally made of Al or FRP.
The challenge is making a structure as light as possible without sacrificing strength. This
requirement leads to stabilize thin surface to with stand tensile and compressive loads and
combination of face sheet and core to resist bending and torsion.
Prepegs
Is ready made type composite available in standard width of 76 to 1270 mm and
thickness varies from 0.1 to 3 mm.
A tape is stored at room temperature or in refrigerator. The resin content varies from 35
to 45%.
Prepegs are in 3 grades
- Continuous fiber embedded in resin matrix
- Discontinuous but aligned fibers embedded in resin matrix.
- Discontinuous and randomly distributed.
Rows of fibers such as glass, aramid, boron or carbon fibers are collected and passed
through collimator with tension rolls. The collimatric fibers pass through resin bath. In
heating chamber curing take place.
Stage A – Un cured stage, where in the resin is to flow easily.
Stage B – Middle stage –Semi viscous to allow process easily. In this stage both
heat and pressure applied.
Stage C – Prepegs become hard and partially cured.
After curing the prepegs pass through take up rolls back with releasing film. The
releasing film keeps prepegs from non-sticking.
Hybrid Composites
Hybrid is obtained by using two or more different types of fiber in a single matrix. A
verity of fiber combinations and matrix materials are used. There are number of ways in
which the two different fibers may be combined.
Fiber may be aligned and intimately mixed with one another.
Laminates may be constructed consisting of layers, each of which consists of single fiber
type, alternating one with another.
Ex – Commonly carbon and glass fiber are incorporated in to a polymeric resin. Carbon
fibers are strong and relatively stiff and provide low density reinforcement. Glass fibers
are inexpensive and lacks of stiffness of carbon. The glass-carbon hybrid is stronger and
tougher has a higher impact resistance and may be produced at lower cost. When hybrid
composites are stressed in tension, failure is usually doesn’t occur suddenly. The carbon
fibers are first to fail, at which the load is transferred to glass fiber. Upon the failure of
glass fiber the matrix phase must sustain the applied load.
Applications-
Light weight land, water, air transport structural components, sporting goods, light
weight orthopedic component.
Desirable characteristics of Fiber Reinforced Composites (Parameters or Factors)
1. Length of fiber
2. Diameter or size of fiber
3. Orientation of fiber
4. Volume fraction of fiber
5. Fiber properties
6. Matrix properties
7. Bonding and Interface strength
Length of fiber:
Usually the ends of fibers have lower load carrying ability and hence higher the ends
lower will be load carrying capacity of the composite. Longer the fiber, number of ends
will be lower and hence higher will be the load carrying capability. It has also been found
that for the same volume fraction of fibers, increasing the length of fibers is found to
increase the tensile strength of fibers.
Diameter of fibers
By reducing the diameter of fibers has following advantages:
The number of flaws is greatly reduced and strength is increased
Contact surface area increased. Smaller the size, more fibers will accommodated
and hence the contact surface is increased which in turn improves the efficiency
of load transfer from the matrix to the fiber.
Flexibility of fibers is greatly increased whereby the fibers can be bent, wound
and woven easily.
Volume fraction
Increasing the volume fraction or amount of fibers lead to increase in the specific
property of the composite. However, maximum volume fraction is restricted to 80% to
ensure that each fiber is surrounded by the matrix phase. It has been found that if the
volume fraction is below 28% the fibers do not effectively reinforce the matrix.
Orientation of fiber
1) Continuous aligned fiber under longitudinal load.
2) Continuous fiber under transverse load.
3) Discontinuous and aligned fiber.
4) Discontinuous and randomly oriented.
Fiber Properties
Fibre reinforcement not only comes in a variety of materials with different strengths and
stiffness, but also in a variety of forms, e.g. mats, straight rovings, woven fabrics. In
some forms the fibres are grossly kinked to conform to a weave pattern and this can
reduce the strength of the composite material. Unlike most conventional materials, the
strength and stiffness of the material can be varied by adjusting the fibre content.
Matrix Properties
The wide variety of polymers with different characteristics is further complicated by the
addition of fillers and Plasticizers which can significantly alter the composite properties. This
can result in published properties being of little value because the exact composition is not
stated or cannot be reproduced. Some matrices may exhibit poor bonding with the fibre
reinforcement and are thus unable to develop the full strength capacity of the fibres.
Bonding and Interface Strength
It is extremely important that the bonding between the reinforcing phase and matrix is
very good. The fibers should not pull out and get de-laminated or de-bonded. To facilitate
good wettability, coupling agents or coatings are used.
1.2 COMPOSITES
1.2.1 Why a composite?
Over the last thirty years composite materials, plastics and ceramics have been the
dominant emerging materials. The volume and number of applications of composite
materials have grown steadily, penetrating and conquering new markets relentlessly.
Modern composite materials constitute a significant proportion of the engineered
materials market ranging from everyday products to sophisticated niche applications.
While composites have already proven their worth as weight-saving materials, the current
challenge is to make them cost effective. The efforts to produce economically attractive
composite components have resulted in several innovative manufacturing techniques
currently being used in the composites industry. It is obvious, especially for composites,
that the improvement in manufacturing technology alone is not enough to overcome the
cost hurdle. It is essential that there be an integrated effort in design, material, process,
tooling, quality assurance, manufacturing, and even program management for composites
to become competitive with metals.
The composites industry has begun to recognize that the commercial applications of
composites promise to offer much larger business opportunities than the aerospace sector
due to the sheer size of transportation industry. Thus the shift of composite applications
from aircraft to other commercial uses has become prominent in recent years.
Increasingly enabled by the introduction of newer polymer resin matrix materials and
high performance reinforcement fibres of glass, carbon and aramid, the penetration of
these advanced materials has witnessed a steady expansion in uses and volume. The
increased volume has resulted in an expected reduction in costs. High performance FRP
can now be found in such diverse applications as composite armoring designed to resist
explosive impacts, fuel cylinders for natural gas vehicles, windmill blades, industrial
drive shafts, support beams of highway bridges and even paper making rollers. For
certain applications, the use of composites rather than metals has in fact resulted in
savings of both cost and weight. Some examples are cascades for engines, curved fairing
and fillets, replacements for welded metallic parts, cylinders, tubes, ducts, blade
containment bands etc.
Further, the need of composite for lighter construction materials and more seismic
resistant structures has placed high emphasis on the use of new and advanced materials
that not only decreases dead weight but also absorbs the shock & vibration through
tailored microstructures. Composites are now extensively being used for rehabilitation/
strengthening of pre-existing structures that have to be retrofitted to make them seismic
resistant, or to repair damage caused by seismic activity.
Unlike conventional materials (e.g., steel), the properties of the composite material can be
designed considering the structural aspects. The design of a structural component using
composites involves both material and structural design. Composite properties (e.g.
stiffness, thermal expansion etc.) can be varied continuously over a broad range of values
under the control of the designer. Careful selection of reinforcement type enables finished
product characteristics to be tailored to almost any specific engineering requirement.
Whilst the use of composites will be a clear choice in many instances, material selection
in others will depend on factors such as working lifetime requirements, number of items
to be produced (run length), complexity of product shape, possible savings in assembly
costs and on the experience & skills the designer in tapping the optimum potential of
composites. In some instances, best results may be achieved through the use of
composites in conjunction with traditional materials.
1.2.2 What is a composite?
A typical composite material is a system of materials composing of two or more materials
(mixed and bonded) on a macroscopic scale.
Generally, a composite material is composed of reinforcement (fibers, particles, flakes,
and/or fillers) embedded in a matrix (polymers, metals, or ceramics). The matrix holds
the reinforcement to form the desired shape while the reinforcement improves the overall
mechanical properties of the matrix. When designed properly, the new combined material
exhibits better strength than would each individual material. As defined by Jartiz, [7]
Composites are multifunctional material systems that provide characteristics not
obtainable from any discrete material. They are cohesive structures made by physically
combining two or more compatible materials, different in composition and characteristics
and sometimes in form. Kelly [8] very clearly stresses that the composites should not be
regarded simple as a combination of two materials. In the broader significance; the
combination has its own distinctive properties. In terms of strength or resistance to heat
or some other desirable quality, it is better than either of the components alone or
radically different from either of them.
Berghezan [9] defines as “The composites are compound materials which differ from
alloys by the fact that the individual components retain their characteristics but are so
incorporated into the composite as to take advantage only of their attributes and not of
their shortcomings”, in order to obtain an improved material
Van Suchetclan [10] explains composite materials as heterogeneous materials consisting
of two or more solid phases, which are in intimate contact with each other on a
microscopic scale. They can be also considered as homogeneous materials on a
microscopic scale in the sense that any portion of it will have the same physical property.
1.2.3 Characteristics of the Composites
Composites consist of one or more discontinuous phases embedded in a continuous
phase. The discontinuous phase is usually harder and stronger than the continuous phase
and is called the ‘reinforcement‘ or ‘reinforcing material’, whereas the continuous phase
is termed as the ‘ matrix’.
Properties of composites are strongly dependent on the properties of their constituent
materials, their distribution and the interaction among them. The composite properties
may be the volume fraction sum of the properties of the constituents or the constituents
may interact in a synergistic way resulting in improved or better properties. Apart from
the nature of the constituent materials, the geometry of the reinforcement (shape, size and
size distribution) influences the properties of the composite to a great extent. The
concentration distribution and orientation of the reinforcement also affect the properties.
The shape of the discontinuous phase (which may by spherical, cylindrical, or rectangular
cross-sanctioned prisms or platelets), the size and size distribution (which controls the
texture of the material) and volume fraction determine the interfacial area, which plays an
important role in determining the extent of the interaction between the reinforcement and
the matrix.
Concentration, usually measured as volume or weight fraction, determines the
contribution of a single constituent to the overall properties of the composites. It is not
only the single most important parameter influencing the properties of the composites,
but also an easily controllable manufacturing variable used to alter its properties.
The orientation of the reinforcement affects the isotropy of the system.
1.3 COMPONENTS OF A COMPOSITE MATERIAL
In its most basic form a composite material is one, which is composed of at least two
elements working together to produce material properties that are different to the
properties of those elements on their own. In practice, most composites consist of a bulk
material (the ‘matrix’), and a reinforcement of some kind, added primarily to increase the
strength and stiffness of the matrix.
1.3.1 Role of matrix in a composite
Many materials when they are in a fibrous form exhibit very good strength property but
to achieve these properties the fibres should be bonded by a suitable matrix.
The matrix isolates the fibres from one another in order to prevent abrasion and formation
of new surface flaws and acts as a bridge to hold the fibres in place. A good matrix
should possess ability to deform easily under applied load, transfer the load onto the
fibres and evenly distributive stress concentration.
A study of the nature of bonding forces in laminates [12] indicates that upon initial
loading there is a tendency for the adhesive bond between the reinforcement and the
matrix to be broken. The frictional forces between them account for the high strength
properties of the laminates.
1.3.2 Materials used as matrices in composites
In its most basic form a composite material is one, which is composed of at least two
elements working together to produce material properties that are different to the
properties of those elements on their own. In practice, most composites consist of a bulk
material (the matrix) and a reinforcement of some kind, added primarily to increase the
strength and stiffness of the matrix.
RULE OF MIXTURES
Rule of Mixtures is a method of approach to approximate estimation of composite
material properties, based on an assumption that a composite property is the volume
weighed average of the phases (matrix and dispersed phase) properties. According to
Rule of Mixtures properties of composite materials are estimated as follows:
Density
dc = dm*Vm + df*Vf
Where
dc,dm,df – densities of the composite, matrix and dispersed phase respectively;
Vm,Vf – volume fraction of the matrix and dispersed phase respectively.