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by Anthony Kelly
The term composite originally arose in engineering
when two or more materials were combined in order
to rectify some shortcoming of a particularly useful
component. For example, cannons which had barrels
made of wood were bound with brass because a hollow
cylinder of wood bursts easily under internal pressure.
The early clipper sailing ships, which were said to be of
composite construction, consisted of wood planking
on iron frames, with the wood covered by copper
plates to counter the attack of marine organisms on
the wood.
For the purposes of this Encyclopedia, a composite
material can be defined as a heterogeneous mixture of
two or more homogeneous phases which have been
bonded together. Provided the existence of the two
phases is not easily distinguished with the naked eye,
the resulting composite can itself be regarded as a
homogeneous material. Such materials are familiar:
many natural materials are composites, such as wood;
so are automobile tires, glass-fiber-reinforced plastics
(GRP), the cemented carbides used as cutting tools,
and paper-a composite consisting of cellulose fibers
(sometimes with a filler, often clay). Paper is essentially
a mat of fibers, with interfiber bonding being provided
by hydrogen bonds where the fibers touch one
another.
It is sometimes a little difficult to draw a distinction
between a composite material and an engineered
structure, which contains more than one material and
is designed to perform a particular function. The
combination is usually spoken of as a composite
material provided that it has its own distinctive
properties, such as being much tougher than any of the
constituent materials alone, having a negative thermal
expansion coefficient, or having some other property
not clearly shown by any of the component materials.
In many cases, the dimensions of one of the phases
of a composite material are small, say between 10 nm
and a few micrometers, and under these conditions
that particular phase has physical properties rather
different from that of the same material in the bulk
form; such a material is sometimes referred to as a
nanocomposite.
The breaking strength of fibers of glass, graphite,
boron and pure silica, and of many whisker crystals, is
much greater than that of bulk pieces of the same
material. In fact, it may be that all materials are at
their strongest when in fiber form. In order to utilize
the strength of such strong fibers, they must be stuck
together in some way: for example, a rope is appropriate for fibers of hemp or flax, and indeed carbon
and glass fibers are often twisted into tows. However,
for maximum utilization, a matrix in which to embed
such strong fibers is required, in order to provide a
The geometrical arrangement of the phases in a composite material can often be described in simple terms
(Fig. 1).
The simplest physical property of a compositenamely its density pc-is given by the volumeweighted average of the densities of the components:
Pc = PI VI + P2V 2
(1)
where V is the volume fraction and subscripts 1
and 2 refer to the components. If there are no voids,
Vt + V 2 = 1. More complicated physical properties,
e.g., those described by a second-rank tensor, relate
two vectors: either a solenoidal vector and an irrotational vector (as with magnetic or electric susceptibility), or else a flux vector and the gradient of a scalar
function (as with diffusivity, and electric and thermal
conductivity). The relations derived for these properties for a composite material in terms of the same
xvii
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0.4
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0.6
0.8
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1.0 r - - - - - - - - - - - - - - - - ,
(d)
(c)
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Figure 1
Composite geometries: (a) random dispersion of spheres in
a continuous matrix; (b) regular array of aligned filaments;
(c) continuous laminae; and (d) irregular geometry (after
Hale 1976)
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(2)
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Figure 2
Dielectric constant of composite materials: (a) el/e2 = 0.1 and
(b) Btle2=0.01. (1) Bounds from Eqns. (1) and (3);(2) Hashin
and Shtrikman bounds for arbitrary geometry (Eqn. (2));(3)
Self-consistent approximation for spheres in a continuous
matrix (after Hale 1976)
posites.
xx
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><
Tahle 1
piezoelectricity
piezoresistivity
stress birefringence
triboluminescence
heat of transition of
pressure- ind uced
phase transition
piezoresistivity and
Joule heating
Electrical (field/
polarization,
current) (3)
Optical and
particle radiation
(light or particle
flux) (4)
Thermal
(tern perat ure,
temperature
gradient, heat
current) (5)
Chemical
(chemical
composition,
chemical
composition
gradient) (6)
Electrical (field/
polarization,
current)(3)
electrostriction
Kirkendall effect
electroviscosity
(suspension)
indirect: thermal
expansion
magnetic susceptibility superconductors
galvanic deposition of
ferromagnetic layer
direct generagtion of
magnetic field
magnetoresistance
dielectric constant,
( + electric current)"
dielectric
polarization
Hall effect ( + electric
current)"
Hall effect
ac resonance
(+ magnetic field)"
induction of voltage
Faraday effect
electroluminescence
magnetooptic Kerr
laser junctions
effect
refractive index
Kerr effect
deflection of
charged particles
absorption by
gal vanic deposits
cold emission of
electrons
adiabatic
dissipation in
demagnetization
resistance
Nernst-Ettingshausen Peltier effect
temperature
Nernst-Ettingshausen
gradient effect (+
temperature
electric current)"
gradient effect ( +
magnetoresistnace
magnetic field)"
effect + Joule
heating ( + electric
field)'
electromigration
galvanic deposition
magnetostriction
magnetoviscosity
(suspension)
Magnetic (field/
polarization)(2)
piezomagnetism
Magnetic
(field/polarization)
(2)
elasticity
Mechanical
(force/
deformation) (1)
Mechanical
(force/
deformation)(I)
field)"
light or particle
stimulated
reactions
(photosensitive
layers)
absorption
ionization
refractive index
fluorescence
scintillation
color-center activation
photoconductivity
photoemission
photoelectromagnetic
effect ( + magnetic
photomagnetic effect
Soret effect
(temperature
gradient)"
phase transition
change of chemical
equilibrium
thermal conductivity
thermoelectricity
ferroelectrics at T~ T;
(+ electric field)"
temperaturedependent resistivity
(+ electric current]"
thermol uminescence
magnetic field)"
atT~Tc(+
thermomagnetism
ferromagnetic material
thermal expansion
Thermal
(temperature,
temperature
gradient, heat
current)(5)
reaction heat
chemoluminescence
dependence of T, on
ferroelectric
composition
dependence of r, on
ferromagnetic
composition
osmotic pressure
Chemical
(chemical
composition,
chemical
composition
gradient)(6)
Matrix classification of some physical properties or phenomena in materials according to the type of input and ouput parameters (after van Suchtelen 1972)
Property of phase
(X-Y)
Property of phase 2
(Y-Z)
Product property
(X-Z)
1-2-3
Piezomagnetism
Magnetoresistance
1-2-4
Piezomagnetism
Faraday effect
1-3-4
1-3-4
Piezoelectricity
Piezoelectricity
Electroluminescence
Kerr effect
2-1-3
2-1-3
Magnetostriction
Magnetostriction
Piezoelectricity
Piezoresistance
2-5-3
N ernst - Ettingshausen
effect
Magnetostriction
Seebeck effect
Piezoresistance
Phonon drag
Rotation of polarization by mechanical
deformation
Piezoluminescence
Rotation of polarization by mechanical
deformation
Magnetoelectric effect
Magnetoresistance
Spin-wave interaction
Quasi-Hall effect
2-1-4
3-1-2
3-1-3
3-4-3
Electrostiction
Stress-induced
birefringence
Piezomagnetism
Electrostriction
Electroluminescence
Piezoresistivity
}
Photoconductivity
3-1-4
Electrostriction
4-2-1
4-3-1
4-3-4
4-4-3
Photomagnetic effect
Photoconductivity
Photoconductivity
Scintillation
Scintillation,
fl uorescence
Stress-induced
birefringence
Magnetostriction
Electrostriction
Electroluminescence
Photoconductivity
FIuorescence
4-4-4
.S-glass
4
E-glass FeeB 2
quartz
steel
Wire
Celion
SiC whisKers
Bon C SiC on C
~gh str~~~ : .
.AS
Bonw. W
Al 20 3 whiskers
Kevlar 4ge
AS-I. .h~:I;O~~~~ Borsic
PEt. AS-2 T-300
Cellon G-50
stainles~ steel T50
-Her;J,;;>H~S
rayon-
CGF~~t~~;C~~5_
Nb_
.Ta
Mo
Fortafd
-Nextal
zr0
T75
, A12 0 3
VCS-32
- P-IOO
-GY-70
Pitch
-SN
Figure 3
20
Kevfar
S-glass
E
u
Celion HTS
15
T-3g0~C- /i~~t:ilskers
quartz
E-glass
T-75 ..
.Bon~ _CG-5.CellonG~0
-AS
~. HMS
T-50 Pan
S~~~I
o ~~~:I. z-o-
Borsic
CG-3
_ A1z03 whiskers
Ne)(tel
VSC-32
GY- 70
Pitch
FeeB z
.AIO
BN - stainless steel
2 3
Mo
~:~
\0
15
20
8
Figure 4
Figure 5
Measured variation of tensile strength with angle c/> for
specimens consisting of a number of alternate layers of
fibers. The fibers in each layer are parallel and
continuous. Alternate layers are at + and at - to the
tensile axis. Open circles represent data for a volume
fraction of 40A> of silica fibers in aluminum. Full circles
represent data for a volume fraction of 66% of E-glass
fiber in an epoxy resin
Fig. 5), being very strong and stiff parallel to the fibers,
but rather weak in shear parallel to the fibers (because
this property depends principally upon the shear
properties of the matrix), and very weak indeed in
tension perpendicular to the fibers. In order to overcome this, the fibers are arranged in laminae, each
containing parallel fibers, and these are stuck together
(Fig. 6) so as to provide a more isotropic material with
a high volume loading of fibers. Figure 6 shows the
specific strengths and stiffness values of laminated
forms of fibrous composites made of some of the fibers
whose properties are shown in Figs. 3 and 4. The
advantage over conventional isotropic constructional
materials represented by the metal alloys is seen to be
considerable but is much less marked than in Figs. 3
and 4.
Alternatively, the fibers may be randomly arranged
in a plane or in three dimensions; such arrangements
limit the obtainable fiber packing density. Fibers are
also often woven into mats before incorporation into
the composite because this aids the handling of fiber
arrays.
When carbon- or other fiber-reinforced plastics are
made with woven fabric rather than nonwoven material, distortion of the load-carrying fibers parallel to
the applied stress reduces the tensile strength further
XXlll
100
(corbon- PEEK)
- Kevlor-epoxy, 0
80
Kevlor-epoxY,1
.corbon-epoxy,O
;::;
bl&
01
40
'u
CLI
B-epoxy,O
8-AI,O
APC-I,2
Kevlar-epoxy, 2
I/)
;;:
corbon-epoxy, I
s- gloss-epoxy, 2
S-gloss-epoxy, I
60
20
a.
TI-6AI-4~AI_Li _Be
steel - _
- a-epoxy, 2
514340)...
- , . carbon-epoxy, 2
AI 7075
(f)
Figure 6
Specific strength and stiffness of some isotropic
materials and of fiber composites. The designation 1 on
the composites means the following arrangements of
fibers: 50% at 0; 40% at 45 and 10% at 90 to the
stress; 2 denotes balanced laminates with equal
proportions at 45, 90 and 135;0 indicates aligned
fibers in the specified matrix. The volume fraction of
fibers in the various composites are not the same in
the different systems. They vary between 40 and 60%.
The metal alloys are those without such designation
3. Applications of Composites
High-performance composites use fibers in order to
attain the inherent properties of the fiber, coupling this
with a judicious choice of matrix so that toughness and
impact damage are not lost.
Strong fibers, whether they be stiff or not, have the
great advantage of restraining cracking in what are
called brittle matrices. It is this use of fibers which is
often referred to when showing how the ancients
employed composite materials. Quotations from the
Bible are made, such as that from the Book of Exodus,
Chapter V, verses 6 et seq., which refer to the difficulty
of making of bricks without straw. Fibers restrain
cracking because they bridge the cracks. The principle
is very simple. It has been used in asbestos-reinforced
cement and the principle of reinforced concrete is not
too far from the same idea. The principle is illustrated
in Fig. 7. A crack passing through a brittle material
may not enter the fibers but leaves a crack straddled by
fibers so that a material which would normally have
broken with a single crack now has to be cracked in a
Without fibers
With fibers
Figure 7
5. Fibers
The very strong and stiff fibers comprise the following,
each with a separate section in this Encyclopedia:
asbestos (a naturally occurring fiber), boron and carbon of varying degrees of graphitization, made in
principle from a number of starting materials but in
practice mainly two: PAN (polyacrylonitrile) and
pitch. Inorganic glasses based on silica yield many
fibers. Those made in the form of continuous filaments
are most important for composite materials. Many
linear polymers such as polyparabenzamide or simple
polyethylene can be processed to form very stiff and
strong fibers. The ways of doing so are very varied.
They are all described in High-Modulus High-Strength
Organic Fibers. Fibers of Al 2 0 3 are important for
high-temperature use in filtration and other applications because of their chemical inertness. These,
and fibers based on silicon carbide and nitride,
again made via various routes, are described in
Oxide Inorganic Fibers, Silicon Carbide Fibers and
Silicon Nitride Fibers, respectively. Whiskers or
tiny (,...... 1 urn diameter) fibers are known of most
materials. They are often very strong and stiff and
possibly will have uses as agents producing toughness, stiffness or wear resistance when introduced
into other materials. Their genesis is described in
Whiskers.
Historically, the first materials designed specifically by chemists to hold fibers in a composite
material were the organic thermosetting resins. The
modern varieties of these resins are described in
7. Properties of Composites
The science of the physical properties of composite
materials relates the properties of the composite to
those of the individual constituents and of the interface
between them. Most of the simple physical properties
such as density, elastic modulus and thermal expansion coefficient can be calculated and, noting the
remarks in Sect 1.1, these calculations and their comparison with experiment are dealt with in Fibrous
Composites: Thermomechanical Properties essentially
for unidirectional fibrous composites. The elastic
properties of laminates which consist of thin layers
(lamellae) stacked upon one another, the fibers being
parallel within each layer, is an important topic for
design and details of how these calculations can be
made appear in Laminates: Elastic Properties. Another
form of arrangement of nonparallel fibers is that of the
woven fabric and the elastic properties of these are
dealt with in Woven-Fabric Composites.Properties.
An engineer may wish to choose a particular
arrangement of fibers of given properties within a
given matrix in order to attain or to approach a
particular set of properties within the composite. For
the simpler properties, where there is confidence in the
prediction of a property from consideration of the
properties of the constituents, such as for elastic
modulus or for thermal expansion coefficient, attainable combinations of properties can be displayed
graphically, leading to the concept of a structureperformance map, described in Structure-Performance
Maps.
Properties such as strength and toughness of composite materials are not as well understood as the
simpler elastic properties because in many cases the
modes of failure under a given system of external load
are not predictable in advance. An added complication
is the fact that the breaking strength of individual
fibers within a population shows a spread of values.
This variation is described generally by what are called
Weibull statistics. Since the breaking strength of a
composite will depend not only on the highest breaking strength of the individual fibers but also on how
the individual breaks are arranged in space within the
composite, the accurate prediction of the breaking
strength requires a complicated statistical theory even
when time-dependent effects are ignored. In the article
Strength of Composites: Statistical Theories, a simplified account of the breaking strenght of unidirectional
composities is given. Despite the complications of
arriving at an exact prediction of the strength, advanced composites are used nonetheless and their
strength measured. Because of the anisotropy of elasticity and strength, these quantities must be measured
in special ways. Methods of achieving reliable
measurements of strength and what simple rules there
are for variation of strength with orientation, fiber
length, and so on are dealt with authoritatively in
Strength of Composites.
I n engineering practice, the static strength of a
composite in the presence of notches and stress concentrations due to geometric form is at least as important as that of simple test pieces used in the laboratory;
a very short account of some important features is
given in Failure of Composites: Stress Concentrations,
Cracks and Notches. In practice, composite materials
must be joined to one another and to other structural
members. The peculiar methods of joining employed
are dealt with in Joining of Composites. Here every
effort is made to minimize stress-concentrating effects
such as abrupt changes of elastic moduli and of
geometrical section or form.
The ability of a material to remain serviceable when
containing cracks, or when cracks arise during service,
depends upon its toughness. It is by no means clear
that measures of toughness or crack resistance, such as
the concept of a critical stress intensity factor derived
from linearly elastic mechanics, are applicable to
composite materials, and some aspects of the problem
are dealt with in Failure of Composites.Stress Concentrations, Cracks and Notches. Some progress can be
made in elucidating the primary mechanisms responsible for the energy required to break a composite
material. These are the sliding friction between fibers
and matrix if broken fibers pull past one another, the
deformation within the fiber and matrix, and the
formation of subsiduary cracks. These energy-dissipating mechanisms depend on the variables of volume
fraction, diameter of fibers, etc., and so representative
diagrams indicating the relative importance of these
can be constructed, as in the article Toughness of
Fibrous Composites.
This description of the mechanical properties of
composite materials has so far made no mention of
time-dependent properties; in particular, strength has
been described almost as a static property. The
strength under oscillating stress is described in Fatigue
of Composites, and the variation of deformation of the
composite with time is described in Creep of Composites. Both are aspects of a general investigative
analysis of the failure of composite materials which has
been called damage mechanics. In Fatigue of Composites, it is shown that emphasis on the strain range to
which a given load subjects a composite can simplify
greatly the interpretation of the results. During cyclic
testing of a composite material, cracks in one of the
constituents occur usually within the matrix. The same
occurs in a static test where it is called multiple
fracture. It is necessary then to understand the physi-
xxvii
Polymer-Matrix Composites).
Bibliography
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Bunsell A R, Kelly A, Massiah A (eds.) 1993 Developments in the science and technology of composite
materials. Proc. 6th European Conf. Composite Materials. Woodhead, Cambridge
Chou T W 1992 Microstructural Design of Fiber Composites. Cambridge University Press, Cambridge
Christensen R M 1979 Mechanics of Composite Materials.
Wiley, New York
Clyne T W, Withers P J 1993 Introduction to Metal Matrix
Composites. Cambridge University Press, Cambridge
Cogswell F N 1992 Thermoplastic Aromatic Polymer
Composites. Butterworth-Heinemann, Oxford
Dhingra A K, Lauterbach H G 1986 Fibers, Engineering. In:
MarIe H F, Bikales N M, Overberger C G, Menges G 1986
Encyclopedia of Polymer Science and Engineering, Vol. 6,
2nd ed. Wiley, New York, pp. 756-802
Gerstle F P Jr 1986Composites In: Marie H F, Bikales N M,
Overberger C G, Menges G 1986 Encyclopedia of Polymer
Science and Engineering, Vol. 3,2nd edn. Wiley,New York,
pp. 776-820
Hale D K 1976 The physical properties of composite materials. J. Mater. Sci. 11: 2105-41
Hannant D J 1978 Fiber Cements and Concretes. Wiley, New
York
Hashin Z, Shtrikman S 1962 A variational approach to the
theory of the effective magnetic permeability of multiphase
materials. J. Appl. Phys. 33: 3125-31
Hull 0 1981 An Introduction to Composite Materials.
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Kelly A 1988 Advanced new materials; substitution via
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XXIX