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Boron Monofilament in Composites

1. The document discusses the manufacturing process of carbon fiber composites. It describes how carbon fibers are made from polyacrylonitrile or pitch precursors through fiberization, stabilization, carbonization, and graphitization processes. 2. The fibers are arranged in laminas containing fibers in either unidirectional or multidirectional orientations. Multiple laminas are stacked and bonded together to form composite laminates. 3. Carbon fibers provide strength and stiffness to composites while the matrix holds the fibers in place and protects them from damage. The manufacturing process orients the carbon atoms in fibers to form strong crystalline structures along their axes.

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0% found this document useful (0 votes)
99 views34 pages

Boron Monofilament in Composites

1. The document discusses the manufacturing process of carbon fiber composites. It describes how carbon fibers are made from polyacrylonitrile or pitch precursors through fiberization, stabilization, carbonization, and graphitization processes. 2. The fibers are arranged in laminas containing fibers in either unidirectional or multidirectional orientations. Multiple laminas are stacked and bonded together to form composite laminates. 3. Carbon fibers provide strength and stiffness to composites while the matrix holds the fibers in place and protects them from damage. The manufacturing process orients the carbon atoms in fibers to form strong crystalline structures along their axes.

Uploaded by

sidharth snath
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

MET416 Composite Materials

Module 2

Types of Fibers used in Composites

1) Fiber – reinforced composite materials consist of fibers of


high strength and modulus embedded in or bonded to a
matrix with distinct interfaces (boundaries) between them.
2) In this form, both fibers and matrix retain their physical and
chemical identities, yet they produce a combination of
properties that cannot be achieved with either of the
constituents acting alone.
3) In general, fibers are the principal load – carrying
members, while the surrounding matrix keeps them in the
desired location and orientation, acts as a load transfer
medium between them, and protects them from
environmental damages due to elevated temperatures and
humidity.
4) Thus, even though the fibers provide reinforcement for the
matrix, the latter also serves a number of useful functions
in a fiber – reinforced composite material.
Basic building blocks in fiber-reinforced composites.

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1. Manufacturing of a composite structure starts with the


incorporation of a large number of fibers into a thin
layer of matrix to form a lamina (ply).
2. The thickness of a lamina is usually in the range of 0.1
– 1 mm (0.004 – 0.04 in.).
3. If continuous (long) fibers are used in make in the
lamina, they may be arranged either in a unidirectional
orientation (i.e., all fibers in on direction) or in a
bidirectional orientation (i.e., fibers in two directions,
usually normal to each other), or in a multidirectional
orientation (i.e.,fibers in more than two directions).
4. A lamina can also be constructed using discontinuous
(short) fibers in a matrix.
5. The discontinuous fibers can be arranged either in
unidirectional orientation or in random orientation.
6. Discontinuous fiber-reinforced composites have lower
strength and modulus than continuous fiber
composites.
7. However, with random orientation of fibers, it is
possible to obtain equal mechanical and physical
properties in all directions in the plane of the lamina.
8. The thickness required to support a given load or to
maintain a given deflection in fiber-reinforced
composite structure is obtained by stacking several
laminas in a specified sequence and then consolidating
them to form a laminate.
9. Various laminas in a laminate may contain fibers either
all in one direction or in different directions.

Fibers


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Fibers are the principal constituents in a fiber – reinforced
composite material.
• They occupy the largest volume fraction in a composite
laminate and share the major portion of the load acting on
a composite structure.
• Proper selection of the fiber type, fiber volume fraction,
fiber length, and fiber orientation is very important, since
it influences the following characteristics of a composite
laminate:

➢ Density
➢ Tensile strength and modulus
➢ Compressive strength and modulus
➢ Fatigue strength as well as fatigue failure mechanisms
➢ Electrical and thermal conductivities
➢ Cost
Carbon Fiber

• Carbon fiber is made of thin, strong crystalline filaments


of carbon that is used to strengthen material.
• Carbon fiber can be thinner than a strand of human hair
and gets its strength when twisted together like yarn.
• Carbon Fiber is a polymer and is sometimes known as
graphite fiber.
• It is a very strong material that is also very lightweight.
Carbon fiber is five-times stronger than steel and twice as
stiff.
• Though carbon fiber is stronger and stiffer than steel, it is
lighter than steel; making it the ideal manufacturing
material for many parts.

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• Carbon fibers are manufactured from two types of


precursors (starting materials), namely, textile precursors
and pitch precursors.
• The most common textile precursor is polyacrylonitrile
(PAN).
• Filaments are wet spun from a solution of PAN and
stretched at an elevated temperature during which the
polymer chains are aligned in the filament direction.
• The stretched filaments are then heated in air at 200 Deg.
C – 300 Deg. C for a few hours.
• At this stage, the CN group s located on the same side of
the original chain combine to form a more stable and rigid
ladder structure.

The molecular structure of PAN, illustrated schematically,


contains highly polar CN groups that are randomly
arranged on either side of the chain. CN is considered a
carbon atom with three single bonds to a nitrogen atom.

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• In the next step, PAN filaments are carbonized by heating


them at a controlled rate at 1000 Deg. C –2000 Deg. C in
an inert atmosphere.
• Tension is maintained on the filaments to prevent
shrinking as well as to improve molecular orientation.
• With the elimination of oxygen and nitrogen atoms, the
filaments now contain mostly carbon atoms.

Conventional PAN Process

• The carbonized filaments are subsequently heat – treated


at or above 2000 Deg. C to make the structure more


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ordered and to turns toward a true graphitic form.
Pitch, a by-product of petroleum refining or coal coking, is
a lower cost precursor than PAN.
• Heating to temperatures above 300 Deg. C, polymerizes
(joins) these molecules into long, two-dimensional sheet
like structures.
• While passing through the spinner et die, the meso-phase
pitch molecules become aligned in the filament direction.
• The filaments are cooled to freeze the molecular
orientation, and subsequently heated between 200 Deg. C
and 300 Deg. C in an oxygen containing atmosphere to
stabilize them and make them infusible (to avoid fusing
the filaments together).
• In the next step, the filaments are carbonized at
temperatures around 2000 Deg. C.
• The rest of the process of trans forming the structure to
graphitic form is similar to that followed for PAN
precursors.
Carbon Fibre Fabrication

Fiberization

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Stabilization

• Before the fibers are carbonized, they need to be


chemically altered to convert their linear atomic bonding
to a more thermally stable ladder bonding.
• This is accomplished by heating the fibers in air to
about 390-590° F (200-300° C) for 30-120 minutes.
• This causes the fibers to pick up oxygen molecules
from the air and rearrange their atomic bonding pattern.
• The stabilizing chemical reactions are complex and
involve several steps, some of which occur
simultaneously.
• They also generate their own heat, which must be
controlled to avoid overheating the fibers.
• Commercially, the stabilization process uses a variety
of equipment and techniques. In some processes, the
fibers are drawn through a series of heated chambers.
• In others, the fibers pass over hot rollers and through
beds of loose materials held in suspension by a flow of
hot air.
• Some processes use heated air mixed with certain
gases that chemically accelerate the stabilization.

Carbonization

• Once the fibers are stabilized, they are heated to a


temperature of about 1,830-5,500° F (1,000-3,000° C) for
several minutes in a furnace filled with a gas mixture that
does not contain oxygen.
• The lack of oxygen prevents the fibers from burning in the
very high temperatures.
• The gas pressure inside the furnace is kept higher than the

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outside air pressure and the points where the fibers enter
and exit the furnace are sealed to keep oxygen from
entering.
• As the fibers are heated, they begin to lose their non-
carbon atoms, plus a few carbon atoms, in the form of
various gases including water vapor, ammonia, carbon
monoxide, carbon dioxide, hydrogen, nitrogen, and others.
• As the non-carbon atoms are expelled, the remaining
carbon atoms form tightly bonded carbon crystals that are
aligned more or less parallel to the long axis of the fiber.
• In some processes, two furnaces operating at two
different temperatures are used to better control the rate
of heating during carbonization.

Graphitization

• The final step in the production of graphite is the


graphitization process
• Amorphous or baked carbon is converted to
electrographite by a thermal treatment at approximately
3000 Degree Celsius.
• Essentially any amorphous carbon material can be
graphitized. The potential crystallite growth and ordering
are latent within the baked carbon structure.
• Under the influence of temperature the crystallites grow
and rearrange in an ordered pattern of stacked parallel
planes. This transformation is accompanied by a change
in the physical properties of the material.
• The greater the degree of crystallite growth during heating
up, the better the graphitability (graphitization degree),
which effects the final resistivity achieved.
• The graphitization degree depends on the structure of the
basic material and the applied graphitization temperature.
• It can be determined by x-ray measurements

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Carbon Fiber –Structure

• Structurally, carbon fibers contain a blend of amorphous


carbon and graphitic carbon.
• Their high tensile modulus results from the graphitic form,
in which carbon atoms are arranged in a crystallographic
structure of parallel planes or layers.
• The carbon atoms in each plane are arranged at the
corners of interconnecting regular hexagons. The
distance between the planes is larger than that between
the adjacent atoms in each plane.
• Strong co-valent bonds exist between the carbon atoms in
each plane, but the bond between the planes is due to van
der Waals - type forces , which is much weaker.
• This results in highly anisotropic physical and mechanical
properties for the carbon fiber.

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Arrangement of carbon atoms in a graphite crystal.

Carbon Fiber – Properties

• High in stiffness
• High in tensile strength
• Has a low weight to strength ratio
• High in chemical resistance
• Temperature tolerant to excessive heat
• Has low thermal expansion

Carbon Fiber – Applications

• Bike frames
• Aircraft Wings
• Automotive drive shafts
• Tubing
• Containers
• Propeller blades
• Car components

Carbon Fiber – Advantages & Disadvantages

Types of Carbon Fibers

Pitch-based CF produces a viscoelastic (pitch) material


through distilling carbon-based materials. Pitch-based

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CF has a higher modulus and is used for manufacturing
in the aerospace industry.

PAN-based CF has greater ability to absorb mechanical


energy (toughness). These materials are used as robust
fibers and are cheaper than pitch-based materials.

Rayon-based CF used for specialized applications like


insulating heat for vacuum furnaces due to heat-
conducting properties.

Mesophase pitch based CF has high thermal


conductivity. Manufacturers use this material within the
field of thermal management.

Cellulose based CF are limited because of their low


carbon yield (10–30 % after carbonization) and they
require hot stretching to enhance mechanical strength
Glass Fiber
• Glass fibers are the most common of all reinforcing fibers
for polymeric matrix composites (PMC).
• The principal advantages of glass fibers are local cost,
high tensile strength, high chemical resistance, and
excellent insulating properties.
• The disadvantages are relatively low tensile modulus and
high density (among the commercial fibers), sensitivity to
abrasion during handling (which frequently decreases its
tensile strength), relatively low fatigue resistance, and
high hardness (which causes excessive wear on moulding
dies and cutting tools).
• It is material made from extremely fine fibers of glass.
• Fiberglass is a lightweight, extremely strong, and robust
material.
• The material is typically far less brittle, and the raw
materials are much less expensive.


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Glass is the oldest, and most familiar, performance fiber.
Fibers have been manufactured from glass since the
1930s.
• Glass fiber products are categorized into four major
groups; chopped strands, direct draw rovings, assembled
rovings, and mat products.
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A-glass: With regard to its composition, it is close to


window glass. It is mainly used in the manufacture of
process equipment.

C-glass: This kind of glass shows better resistance to


chemical impact.

D- Glass: Boron trioxide is used as a starting material for


the synthesis. Other boron compounds such as boron
carbide used in the production. High heat resistance and
thermal shock resistance borosilicate glasses.

E-glass: This kind of glass combines the characteristics


of C-glass with very good insulation to electricity. E-glass
is basically a calcium alumino-borosilicate glass
containing less than 1% alkali calculated as Na2O.
Glass Fiber – Fabrication

• Various ingredients in the glass formulation are first dry-


mixed and melted in a refractory furnace at about 1370
Deg. C.
• The molten glass is exuded through a number of orifices
contained in a platinum bushing and rapidly drawn into
filament s of ~10 mm in diameter.

• It is made from silica glass in a special manner, by forcing


the molten glass through fine apertures under high
pressure, when thread like mass is obtained.
• It is made either in the form of continuous strands alike
silk or in the staple form just like wool.
• A protective coating (size) is then applied on individual
filaments before they are gathered together into a strand
and wound on a drum.

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• The coating or size is a mixture of lubricants (which


prevent abrasion between the filaments), antistatic
agents (which reduce static friction between the
filaments), and a binder (which packs the filaments
together into a strand).
• It may also contain small percent ages of a coupling agent
that promotes adhesion between fibers and the specific
polymer matrix for which it is formulated.
Output of forming Stage
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• The basic commercial form of continuous glass fibers is
a strand, which is a collection of parallel filaments
numbering 204 or more.
• A roving is a group of untwisted parallel strands (also
called ends) wound on a cylindrical forming package.
• Rovings are used in continuous moulding operations,
such as filament winding and pultrusion.
• They can also be pre-impregnated with a thin layer of
polymeric resin matrix to form prepregs. Prepregs are sub
sequentially cut into required dimensions, stacked, and cu
red into the final shape in batch moulding operations, such
as compression moulding and hand layup moulding.
• Chopped strands are produced by cutting continuous
strands into short lengths.
• Chopped strands ranging in length from 3.2 to 12.7 mm
(0.12 5–0.5 in.) are used in injection - moulding
operations.
• Longer strands, up to 50.8 mm (2 in.) in length, are mixed
with a resinous binder and spread in a two – dimensional
random fashion to form chopped strand mats (CSMs).
• Glass fibers are also available in woven form, such as
woven roving or woven cloth.

Glass Fiber – Structure

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A typical molecular structure of an amorphous glass
fiber containing silica network

Glass Fiber – Properties

Physical Strength: Fiberglass has a greater strength-to-


weight ratio than steel. This makes it ideal for producing
high-performance materials.

Electrical properties: Fiberglass is an excellent electrical


insulator even at low thicknesses.

Non-combustible: Fiberglass has the advantage of being


naturally non-combustible because it is a mineral
material. Flame cannot spread or be sustained by it.
Fiberglass does not burn, smoke, or emit toxic
compounds when heated.

Fiberglass is not affected by changes in temperature and


humidity.

Organic compatibility: Fiberglass can have various sizes


and can be combined with a wide range of synthetic resins
and mineral matrices like cement.

Durable: Fiberglass is resistant to decay and is unaffected


by pests and rodents.

Thermal conductivity: Fiberglass has a low thermal


conductivity that makes it ideal for use in construction.

Dielectric permeability: Fiberglass is suitable for


electromagnetic windows due to its insulating properties.
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Glass Fiber – Applications

Construction: Fiberglass is used in house building as well


as flat roofing.

Transportation: Fiberglass is extensively used in


transportation. Fiberglass components can be found on
almost every make and model of vehicle, including body
parts & panels

Aerospace & Defence: A wide range of products, including


test equipment, ducting, enclosures, and more, are made
from Fiberglass.

Beverage industry: Fiberglass is used in bottling lines and


brewing houses.
Chemical industry: In this industry, fiberglass grating,
mixed with resin, is used as an anti-slip safety feature.

Marine Industry: Fiberglass is used as a protective


material in docks and marinas to prevent salty seawater
from causing damage, such as rust and corrosion.

Food processing: Fiberglass is used for slip resistance


and prevents machine corrosion from blood in food
processing plants.

Aquaria & Ponds: Many garden ponds are also


constructed from fiberglass due to its water resistance.

Glass Fiber – Advantages & Disadvantages

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Different Forms of Glass Fibre available in market

Natural Fibers
• Examples of natural fibers are jute, flax, hemp, ramie, sisal,
coconut fiber (coir), and banana fiber (abaca).
• All these fibers are grown as agricultural plants in various
parts of the world and are commonly used for making
ropes, carpet backing, bags, and so on.
• The components of natural fibers are cellulose
microfibrils dispersed in an amorphous matrix of lignin
and hemicellulose.
• Depending on the type of the natural fiber, the cellulose
content is in the range of 60 – 80 (weight %) and the lignin
content is in the range of 5 – 20 (weight %).
• In addition, the moisture content in natural fibers can be
up to 20 (weight %).

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Types of Natural Fibers:

There are two types of natural fibers that are discussed


below.

➢ Plant Fiber: Plants fibers are obtained from various parts


of plants like leaves, wood, fruits, flowers, stems etc.
➢ Animal Fiber: Animal fibers are extracted from animals
like silk, wool, etc.

The natural fibers names are given below:

Wood: From wood, we get softwood and hardwood


Stem/Bast: From stem, we get flax, jute, hemp, kenaf, and
ramie
Leaf: From leaf, we get sisal, abaca, pineapple, banana,
palm, fique, henequen
Seed/Fruit: From seed, we get cotton, coconut
Grass: From grass, we get bamboo, rice
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Animals: From animals, we get wool, silk, angora, mohair
etc.
Boron Fiber

• Boron has been utilized in many different fields. One of


these areas is boron fiber.
• Boron fiber is a kind of metallic fiber consisting of boron
atoms in ribbon form.
• The most prominent feature of boron fibers is their
extremely high tensile modulus, which is in the range of
379–414 GPa.
• Coupled with their relatively large diameter, boron fibers
offer excellent resistance to buckling, which in turn
contributes to high compressive strength for boron fiber-
reinforced composites.
• The principal disadvantage of boron fibers is their high
cost, which is even higher than that of many forms of
carbon fibers.
• For this reason, its use is at present restricted to a few
aerospace applications.

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Boron fibers are manufactured by chemical vapour
deposition
• (CVD) of boron onto a heated substrate (either a tungsten
wire or a carbon monofilament).
• The most common substrate used in the production of
boron fibers is tungsten wire, typically 0.0127 mm (0.0005
in.) indiameter.
• It is continuously pulled through a reaction chamber in
which boron is deposited on its surface at 1100 Deg. C –
1300 Deg. C.
• The speed of pulling and the deposition temperature can
be varied to control the resulting fiber diameter.
• Currently, commercial boron fibers are produced in
diameters of 0.1, 0.142, and 0.203 mm (0.004, 0.0056, and
0.008 in.), which are much larger than those of other
reinforcing fibers.
Boron Fiber – Properties

• These are ceramic monofilament fiber with Circular cross


section.
• Boron is brittle hence large diameter results in lower
flexibility.
• Thermal coefficient mismatch between boron and
tungsten results in thermal residual stresses during
fabrication cool down to room temperature.
• Boron fibers are usually coated with Silicon Carbide. So
that, it protects the surface during contact with molten
metal when it is used to reinforce light alloys. Further, it
avoids the chemical reaction between the molten metal
and fiber.
• Strong in both tension and compression.
• Exhibits linear axial stress-strain relationship up to 650
Deg. C.

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Boron Fiber Fabrication
• The CVD (Chemical Vapor Deposition) is a process in
which one material is deposited onto a substrate to
produce near theoretical density and small grain size for
the deposited material.
• In CVD the material is deposited on a thin filament.
• The material grows on this substrate and produces a
thicker filament.

• The passage taken place for Few mins


• During the process, atoms diffuse into tungsten core to
produce complete boridization
• Formation of WB4 and W2B5 occurs
• The size of the final filament is such that it could not be
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produced by drawing or other conventional methods of
producing fibers.
• It is the fine and dense structure of the deposited material
which determines the strength and modulus of the fiber.
• Boron Fiber is produced in single-filament reactors by
chemical vapor deposition, boron fiber exhibits a unique
combination of high compression strength, high modulus
and large diameter.
• It provides superior compression properties compared to
carbon fiber based composites.
• Elemental boron is deposited on a fine tungsten wire
substrate and produced in diameters of 102-micron and
142-micron.
• The resulting fiber is essentially amorphous boron with a
fully borided-tungsten core.
Boron Fiber – Structure

• Elemental boron is deposited on a fine tungsten wire


substrate and produced in various dia
• The resulting fiber is essentially amorphous boron with a
fully borided tungsten core
• Thermal coefficient mismatch between boron and
tungsten results in thermal residual stresses during
fabrication cool down to room temperature.
• Boron fibres are usually coated with SiC or so that it
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protects the surface during contact with molten metal
when it is used to reinforce light alloys. Further, it avoids
the chemical reaction between the molten metal and fibre.

Boron Fiber –Applications


Properties of Boron Fiber

• Boron fiber exhibits a unique combination of high


compression strength, high modulus and large
diameter.
• It provides superior compression properties compared
to carbon fiber-based composites.
• No other composite material has higher compressive
strength properties than Boron fiber & boron fiber
composites
• When using boron fiber composites, a designer can
reduce the laminate thickness resulting in higher
performance at a lower mass
• Hy-Bor® is used in space applications like the Google
Earth Cameras because its zero CTE & High Elastic
Modulus
• No galvanic corrosion with boron fiber

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Boron Fiber – Advantages & Disadvantages
Aramid Fiber

• Aramid fibers are highly crystalline aromatic polyamide


fibers that have the lowest density and the highest tensile
strength – to – weight ratio among the current reinforcing
fibers.
• Kevlar 49 is the trade name of one of the aramid fibers
available in the market.
• As a reinforcement, aramid fiber s are used in many
marine and aerospace applications where light weight,
high tensile strength, and resistance to impact damage
(e.g., caused by accidentally dropping a hand tool) are
important.
• Like carbon fibers, they also have a negative coefficient of
thermal expansion in the longitudinal direction, which is
used in designing low thermal expansion composite
panels.
• The major disadvantages of aramid fiber – reinforced
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composites are their low compressive strengths and
difficulty in cutting or machining.
• There are two main types of aramid fibers.

➢ Meta- aramid
➢ Para- aramid

• The term meta and para refers to the location of chemical


bonds in the structure of aramid fibers.

• The chemical bonds of a para-aramid fibers are more


aligned in the long direction of the fibers.
• The meta-aramid fibers are not aligned they are in zigzag
pattern there for they are not developed the higher tensile
strength of the para-aramid bonds.
• Different trade names of aramid fibers are Kevlar,
Technora, Tawron, Nomex etc.
Aramid Fiber – Structure

• Structure consists of relatively rigid polymer chains with


linked benzene rings and amide bonds.
• The molecular structure of aramid fibers, such as Kevlar
49 fibers, is given below

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• The repeating unit in its molecules contains an amide (–


NH) group (which is also found in nylons) and an aromatic
ring.
• The aromatic ring gives it a higher chain stiffness
(modulus) as well as better chemical and thermal stability
over other commercial organic fibers, such as nylons.
Aramid Fiber – Fabrication

• Kevlar 49 filaments are manufactured by extruding an


acidic solution of a proprietary precursor (a
polycondensation product of terephthaloyol chloride and
p-phenylene diamine) from a spinneret.

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• During the filament drawing process, Kevlar 49 molecules


become highly oriented in the direction of the filament
axis.
• Precipitation bath contains ammonia like chemical
solution.
Aramid Fiber – Properties

• Form strong bonds that are resistant to heat.


• Aramid fibers have medium to ultra-high strength,
medium to low elongation and moderately high to ultra-
high modulus.
• All aramids contain amide links that are hydrophilic.
However, not all aramid products absorb the same
moisture.
• They burn only with difficulty because of limited oxygen
Index values.
• High Strength.
• Good chemical resistance.

Aramid Fiber – Applications

• It is usually used as fiber reinforcement for polymer matrix


composites.

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Ballistic protective applications such as bullet proof vests.
Protective apparel such as gloves and motorcycle
protective clothing.
• Sails for sailboats, yachts etc.
• Belts and hosing for industrial and automotive
applications.
• Aircraft body parts and Boat hulls.
• Fiber optic and electromechanical cables.
• Friction linings such as clutch plates and brake pads.
• Gaskets for high temperature and pressure applications.

Aramid Fiber – Advantages & Disadvantages


Whiskers

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a) Continuous long fibers b) whiskers/short fibers c)
particles

• Whiskers are monocrystalline, short fibers with extremely


high strength.
• This high strength, approaching the theoretical strength,
comes about because of the absence of crystalline
imperfections such as dislocations.
• Being monocrystalline, there are no grain boundaries
either.
• Typically, whiskers have a diameter of a few μm and a
length of a few mm.
• Their aspect ratio (length/diameter) can vary between 50
and 10,000.
• Whiskers, however, do not have uniform dimensions or
properties.
• This is perhaps their greatest disadvantage, i.e., the
variability in properties is extremely large.
• Handling and alignment of whiskers in a matrix to produce
a composite are other problems.

Whiskers – Properties & Characteristics

• High strength
• High Chemical Resistance
• High Thermal Resistance

➢ When it is used as a reinforcement material for composite


materials, its high aspect ratio improves those
mechanical properties.
➢ It is chemically stable
➢ It can be used in ceramics which contact with food
directly.
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➢ It can be dispersed in water.
➢ It has very high dielectric constant.

Whiskers – Applications

• Reinforcement materials for hard ceramics used in cutting


tools – For turbines and jet engines.
• Reinforcement materials for hard ceramics for wear
resistant applications – Excellent abrasion resistance
than hardened steels.
• Ceramics capable of microwave heating – For cooking
and industrial heating.
• Reinforcement materials for plastics.
Whiskers – Advantages & Disadvantages

Advantages:

• High moduli strengths and low densities


• Resist temperature, mechanical damage and oxidation
• Strength varies inversely with effective diameter

Disadvantages:

• No unform properties
• Handling is difficult

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Common questions

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PAN-based carbon fibers utilize polyacrylonitrile as their precursor, whereas pitch-based fibers use mesophasic pitch material. PAN fibers undergo a chemical alteration where linear atomic bonds convert into stable ladder bonds through heat treatment, initially at 200-300°C, followed by carbonization at 1000-2000°C. This leads to carbon filaments with high tensile strength and better toughness, making them cheaper and suitable for robust fiber applications . In contrast, pitch-based carbon fibers are less expensive sources but are processed to align molecules before carbonization, yielding high modulus properties suitable for aerospace applications due to their stiffness and rigidity . These structural differences result in PAN-based fibers being favored for general robustness and cost-effectiveness, while pitch-based fibers are chosen for applications requiring superior stiffness.

Economic factors such as cost of production, availability, and performance requirements significantly influence fiber selection. Carbon fibers, despite their high cost due to energy-intensive production processes, offer an excellent balance of strength, weight, and versatility, making them popular for various high-performance applications like aerospace and automotive industries . Boron fibers are even costlier due to the meticulous CVD process and the use of tungsten substrates, thus are reserved for specialized uses where their exceptional compressive strength justifies the investment, such as in specific aerospace applications . Aramid fibers, being lighter and known for their impact resistance, are less expensive than carbon and boron fibers, providing a cost-effective alternative for applications where tensile strength and light weight are crucial, such as in protective gear and marine industries . Overall, the economic decision balances initial material costs with long-term performance and lifecycle considerations, heavily dictated by the specific demands of the application.

In carbon fiber production, the thermal stabilization process involves heating PAN fibers in air at 200-300°C for up to 120 minutes to introduce oxygen molecules, stabilizing their atomic structure and preventing fusion during subsequent processes . For boron fibers, stabilization is not explicitly mentioned because the process involves chemical vapor deposition (CVD) at high temperatures (1100-1300°C) to deposit boron onto a tungsten or carbon substrate . The absence of a direct stabilization step in boron fibers results in their high compressive strength and stiffness due to the immediate formation of a ceramic layer, whereas carbon fiber stabilization affects their tensile strength by aligning molecular bonds, providing high tensile modulus but lower compression strength than boron fibers.

Natural fibers, such as flax and hemp, are derived from renewable plant sources and are biodegradeable, offering significant environmental benefits over synthetic fibers. They require less energy for production and emit lower greenhouse gases. Economically, they are generally lower in cost due to abundant raw materials, but have limitations in mechanical properties compared to synthetic fibers . In contrast, synthetic fibers like carbon fibers offer superior strength-to-weight ratios, durability, and are not susceptible to the same environmental degradation, which justifies their high cost for high-performance applications like aerospace . However, carbon fiber production is energy-intensive and poses greater environmental impacts. Industries must balance these considerations by evaluating lifecycle impacts, intended fiber application, and regulatory compliance with sustainable practices.

Aramid and carbon fibers both display low thermal expansion, but the nature of this property influences their use differently in composite materials. Aramid fibers possess a negative coefficient of thermal expansion longitudinally, which contributes to maintaining dimensional stability under temperature variations, particularly beneficial in designing composite panels to minimize thermal deformation . Carbon fibers also exhibit low thermal expansion due to strong intra-planar atom bonds within graphitic planes, making them suitable for aerospace and automotive applications where thermal stability is crucial . The combination of these fibers in composites allows for optimization of thermal and mechanical stability under diverse operational conditions, crucial for performance-critical parts such as aircraft wings and satellite components.

Boron fibers offer superior compressive strength and modulus compared to carbon fibers due to their ceramic monofilament nature and high diameter, which enhances buckling resistance. This makes them ideal for applications requiring high compressive properties like space instrumentation and certain aerospace structures . However, boron fibers are significantly more costly than carbon fibers, limiting their widespread use. Carbon fibers, while offering excellent tensile strength-to-weight ratio and overall structural integrity, lack the same compressive capabilities of boron fibers, but are more economically viable for mass production . This makes carbon fibers more appropriate for commercial applications like automotive parts and sports equipment where affordability and tensile performance are prioritized over compressive strength.

Molecular orientation plays a crucial role in determining the mechanical properties of both carbon and aramid fibers. In carbon fibers, such as those derived from PAN precursors, fibers are wet-spun and stretched during processing, aligning the polymer chains in the direction of the filament. This alignment enhances their strength and tensile modulus by ensuring that stress is distributed evenly across similarly oriented chains . In aramid fibers, like Kevlar, the molecular structure involves oriented benzene rings and amide bonds, providing high tensile strength-to-weight ratios. The para-aramid fibers exhibit chemical bond alignment in the fiber long direction, yielding higher tensile strength, while meta-aramid fibers lack such alignment, resulting in lower mechanical properties . This orientation is pivotal for applications demanding high performance under stress, such as aerospace and military materials, due to the reinforcement provided by aligned molecular structures.

The chemical vapor deposition (CVD) process is central to boron fiber production, where boron atoms are deposited on a tungsten substrate within a high-temperature reaction chamber. This method ensures high purity, near-theoretical density, and fine grain structure of the boron layer, crucial for achieving the desired mechanical properties, particularly high compression strength and modulus . CVD allows precise control over fiber diameter, important for maintaining uniformity and strength properties across different batches. These properties make boron fibers particularly effective in aerospace applications despite their high cost, as they meet the stringent demands for mechanical resilience under compressive loads.

Meta-aramid fibers feature a zigzag chemical bond arrangement, while para-aramid fibers have bonds aligned in the fiber's longitudinal direction. This alignment in para-aramids, such as Kevlar, results in significantly higher tensile strength compared to meta-aramids . The structural differences are due to the variation in chemical processing: para-aramids are often extruded from a solution that promotes linear molecular alignment. This molecular orientation enhances the performance of para-aramids in applications demanding high tensile strength and impact resistance, such as ballistic armor and aerospace materials. Meta-aramids, having lower tensile strength, are utilized where flame resistance and thermal stability, rather than mechanical strength, are paramount, such as in firefighting suits and heat-resistant fabrics. These fabrication and structural distinctions fundamentally determine their respective applications based on the performance requirements.

The anisotropic nature of carbon fibers, due to their structured parallel graphitic planes with co-valent intra-planar bonds and weaker inter-planar van der Waals forces, results in high strength and stiffness predominantly in the direction of the fibers. This characteristic enables their use in applications where directional strength is critical, such as in aerospace and automotive industries, where components like aircraft wings, automotive drive shafts, and bike frames must withstand significant loads with minimal weight . The anisotropy allows these industries to design materials that optimize load-bearing capabilities while maintaining lightweight structures critical for enhancing fuel efficiency and performance.

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