Textile Fibre Properties and Structure
Introduction
The study of the structure & physical properties of fibers, yarns & fabrics forms the unified subject that is legitimately. It is an essential part of education of any textile technologist.
Physical structure of fibres
Crystallinity
and orientation, Basic concepts of methods for investigating fibre structure,
e.g. X-ray diffraction, optical and electron microscopy infra-red absorption,
relations between fibre properties and structure of fibre.
Detailed study of fibre properties
Mechanical properties –
tensile, flexural and torsional properties, stress/strain relations under
various conditions, Modules of elasticity, plasticity, creep and relaxation.
Effects of moisture – Effect
of water on fibre e.g. swelling.
Frictional properties –
Importance in drafting experimental methods of measurement. Effect of lubricant
and dyes.Relationship of frictional properties of knitting, stitching and
sewing.
Optional properties –
Reflection, refraction, scattering, polarization, birefringence.
Thermal properties –
Absorption and emission of radiation, Energy changes asociated with changes of
state including transition temperature of fibres. Moisture content and heat of
wetting
Physical structure of fibres
Crystallinity and orientation, Basic concepts of methods for
investigating fibre structure, e.g. X-ray
diffraction, optical and electron microscopy infra-red
absorption, relations between fibre properties and structure of fibre.
Detailed study of fibre properties
Mechanical properties – tensile, flexural and
torsional properties, stress/strain relations under various
conditions, Modules of elasticity, plasticity, creep and
relaxation.
Effects of moisture – Effect of water on fibre e.g.
swelling.
Frictional properties – Importance in drafting
experimental methods of measurement. Effect of
lubricant and dyes.Relationship of frictional properties of
knitting, stitching and sewing.
Optional properties – Reflection, refraction, scattering,
polarization, birefringence.
Thermal properties – Absorption and emission of
radiation, Energy changes asociated with changes of
state including transition temperature of fibres. Moisture
content
Parameters/properties
of textile materials
1. Strength (tensile,
tearing, bursting)
2. Durability
(serviceability)
3. Longevity (more than
it can perform)
4. Degradation
5. Weight
6. Thickness
7. Pliability
8. Absorbency
(modalÃ
regenerated, more
absorbency, more
strength)
9. Air permeability
10. Stiffness
11. Softness
12. Compressibility
13. Elasticity
14. Extensibility
15. Friction/surface
characteristics
16. Electrical
17. Thermal
18. Crease resistance
19. Crease recovery
(Cotton bad crease
recovery, polyester
good crease
recovery)
20. Drape
21. Luster
22. Regain
23. Handle
24. Breaking length
25.
Water resistance
Factors
on which properties of textile materials depend
i. Fibres
properties
a. Chemical
content
b.
Molecular wt./chain length
c.
Molecular arrangement
ii. Yarn
properties
a. Fibres
properties
b. Fibres
arrangement
c. TPI
iii. Fabric
construction
a. EPI
b. PPI
c. Warp
count
d. Weft
count
iv. Fabric
structure
a. Woven
fabrics (plain, twill, satin etc.)
b. Knit
fabrics (plain, rib, interlock, purl, warp)
c.
Felting/bonding
d. Braiding
v. Fabric
engineering
a. Yarn
specification
b. Fabric
specification
c. Yarn
crimp
d. Weave
structures
vi. Fabric
finishing
a.
Mechanical and chemical
Properties of fibres depends on the following
a. Chemical
constitution and properties
b.
Molecular structure and dimension
c.
Arrangement of fibres forming molecules
d.
Auxiliaries used for fibres manufacture
e. Conditions and technique of man-made
fibres manufacturing
Fibre
Fibre
By Textile
Institute fibre is defined as units of matter characterized by flexibility,
fineness and a high ratio of length to thickness (1000:1). For textile fibres a
sufficient high temperature stability and a certain minimum strength and
extensibility required. Elastic upto breaking extension 5-50%. Since glasses
and crystalline solid are less extensive whereas rubber are much more
extensible. Cellulose, proteins and variety of synthetic fibres are partly
oriented, partly crystalline linear polymers.
Fibre
structure depends on the following information
1.
Chemistry of fibre material (preparation, composition, molecular
formula and reaction)
2.
Absorption of infrared radiation
3.
Optical and x-ray diffraction studies
4.
Optical properties
5.
Optical microscopy
6.
Electron microscopy/diffraction
7.
Thermal analysis
8.
Density
9.
Nuclear magnetic resonance
10.
General physical properties.
Crystallinity
If a
substance exposed to x-rays, gives sharp and well defined x-ray diffraction
patterns, then the substance is called crystalline substance and this property
is called crystallinity.Maximumcrystallinity is possible if the polymer is
annealed just at its melting temperature for sufficient long time.
Crystallinity is expressed as degree of crystallinity as below,
Degree of crystallinity = here, C- refraction Index,
Ccr –the value of property when the polymer
is crystalline, Cam- the value of property when the
polymer is amorphous.
Amorphousness
If a
substance exposed to x-rays, gives diffused and broad x-ray diffraction
patterns, then the substance is called amorphous substance and the property is
called amorphousness.
Orientation
The
molecular orientation of fibre is the alignment of long chain molecules
relative to the fibre axis. When the molecules of a material are highly
oriented they are parallel to each other and parallel to the axis of fibre.
There is no 100% crystalline or 100% amorphous material.
Requirements
of fibre formation
1.
Polymer must have straight and long chain molecules
2.
The chain must be more parallel to one another
3.
Molecular weight of the polymer should be high (DP)
4.
Polymer must have attraction among the molecules
5.
Polymer should have resistance to different chemicals
6.
Polymer should be soluble in some solvents from which it can be
spun(not for melt)
7.
Hygroscopic nature of the polymer should be hydrophilic
8.
There should be freedom in molecular movement in order to give required
extensibility.
Methods
for investigation of fibre structure
1.
X-ray diffraction method
2.
The absorption of infra-red radiation
3.
Optical microscopy
4.
Electron microscopy
5.
Nuclear magnetic resonance
X-ray diffraction method
When
a beam of x-ray strikes on a crystal, it strongly reflects and it strikes on
the layers of atoms
at a certain
angle θ. In this case, initial angle is equal to reflected angle.Let the
distance between atomic layers=d, wave length of x-ray =λ
Here,
<FBD =900 and <FBC =θ So, <CBD=90-θ, As, <BCD=900 So, <CBD
+ <BDC = 90 => 90- θ+ <BDC = 90 =><BDC = θ
Now, sinθ= => BC =BDsinθ =dsinθ.
Again,
<FBD= 900 and <EBA =θ, so, <ABD = 90-θ and similarly,
<BDA =θ
Now, sinθ=
=> AB=BD sinθ =dsinθ Now, AB + BC = dsinθ + dsinθ =2dsinθ
ð Nλ=2dsinθ.
Where, n be the integer no.
So, if d is greater atomic layer distance increased
but crystallinity decrease.
When
infrared radiation composed of electromagnetic waves with wavelengths between 1
and 5µm is passed through a material, it is mostly highly absorbed at certain
characteristic frequency. By using an infrared spectrometer, the radiation in
absorption can be found and plotted against wave number. This is illustrated in
the following which is absorption spectrum of nylon.
Here,
full-line represents electric vector perpendicular to fibre axis and broken
line represents electric vector parallel to fibre axis.
The peaks
occur where the frequency of the electromagnetic waves corresponds with the
natural frequency of vibration between two atoms in the material. If these are
associated with electric dipole then the vibration of electric field set up the
vibration and energy is absorbed from the radiation.
The wave no.
at which absorption takes place depends primarily on the nature of the two
atoms and of the bond between the, =NH, =CO,ΞC-CΞ,=C=C=, -OH, ΞC-O- etc.
To similar extent, the absorption frequency is
influenced by the other groups in the neighborhood.
Instrument consist of-
1.
Source of infrared radiation
2.
Diffraction grating
3.
Sensitive heat detector
4.
Output display.
Advantages
of infrared radiation absorption method
1.
The first use of infrared absorption is an aid to the
identification of the presence of certain groups in the molecule, leading to
the determination of its chemical formula
2.
The method can be used in routine analysis to identify
and estimate quantitatively the presence of given substance, even in small
quantities in a mixture
3.
It can be used to determine the amount of water in fabrics.
4.
It can analyze the degree of orientation of molecules in a fibre
5.
It can determine the molecular configuration of a molecule.
6.
It can give information about molecules of crystalline and
non-crystalline region.
Electron microscopy
Electrons
are particles that can act as if they were waves with a wavelength of order of
0.005nm; and furthermore they can be focused since their path [rays] can be
bent by electric and magnetic fields in the same way that light rays are bent
by lenses. It is therefore possible to form an image by an electron microscope
with a limit of resolution that is far smaller than is possible with an optical
microscope.
Why?
-
Allows a sample to be examined at far higher
magnification and lateral resolution than is possible with light microscopy
-
Large depth of field/whole surface remaining in focus
at a time
-
Huge range of contrast
The electron microscope
illustrated schematically in the following figure is
exactly
analogous to the optical microscope. The rays from an electron source are
condensed on the specimen and then focused by electric or magnetic fields
acting as lenses to give a magnetic image on a fluorescent screen or
photographic plate.
Difficulties
-
Obtaining sufficient contrast
-
Ordinary transmission/confusion of depth of focus
-
Observed may be caused by the section-cutting [for high contrast]
Uses
-
Cut face/fibre structure
-
Internal details may also be shown by peeling a layer a
layer off the fibre to expose a new internal surface for replication.
-
Fragments left behind after mechanical/chemical degradation
-
Information same as X-ray diffraction [orientation/crystalline]
Types
1.
Scanning electron microscope [detector mounted on the same side of the
sample]
Condenser lens
-
Create a de-magnified image f the gun crossover
-
Control minimum beam spot size
-
Affects the beam convergence at the sample
-
Controls diameter of the illuminated area
Aperture
-
Control the intensity of illumination
Objective lens
-
Form an inverted initial image which is subsequently magnified
-
Form a diffraction pattern in the back focal plate
Objective Aperture
-
Selects electrons that will contribute to the image
-
Improves contrast of the final image
-
Placed in back plane of image
Intermediate lens
-
Magnify initial image formed by objective lens
-
Focuses on initial image or diffraction pattern formed
in back focal plane
Projector lens
-
Magnifies size of image
-
Can have various strength
Relation
between fibre properties and structure
1.
Tensile strength is –
a.
Proportional to covalent bond energy
b.
Proportional to molecular weight
c.
Proportional to crystallinity
d.
Proportional to fibre orientation
2.
Extensibility is-
a.
Reciprocal to degree of molecular orientation
b.
Reciprocal to degree of crystallinity
c.
Proportional to helical angle of fibril
d.
Proportional to chain length
3.
Moisture regain is-
a.
Proportional to no. of polar group
b.
Reciprocal to degree of crystallinity
4.
Electric property is-
a.
Proportional to degree of crystallinity
b.
Proportional to molecular orientation
5.
Electric conductivity is-
a.
Reciprocal to degree of crystallinity
b.
Proportional to no. of polar group
c.
Proportional to electrolytic content
1.
Mechanics of Yarn and Fabric Structure and Properties- J.W.S. Hearle
2.
Physical Testing of Textiles-B.P. Saville.
3.
Proper properties of textile fibre- Morton.
4.
Principle of Textile Testing- J.E. Booth
5.
Man-made Fibres- Moncrif