Textile Fibers Ist Sem TT Notes 1
Textile Fibers Ist Sem TT Notes 1
SUBJECT
TEXTILE FIBRES
2022
Compiled By:
1. Dr. Rajesh Kadian, Sr. Lect. Govt. Polytechnic, Hisar
2. Er. Puneet Garg, Sr. Lect. Govt. Polytechnic, Jattal
3. Er. Krishan Kumar, Lect. Govt. Polytechnic, Jattal
4. Er. Rakesh Jindal, Lect. Govt. Polytechnic, Hisar
Subject -1.5 TEXTILE FIBRES
Unit-I INTRODUCTION
Syllabus - General concept of Textile, fiber, yarn, fabrics and wet processing. Definition of Textile
fiber and filament. Classification of Textile fibers according to nature and origin. General physical
properties of Textile Fibers. General chemical properties of Textile Fibers.
NATURAL FIBERS:
1. Vegetable Fibers – Cotton, Jute, Flax, Coir, Hemp, Ramie etc.
2. Animal Fibers - Wool, Silk, Mohair etc.
3. Mineral Fiber – Asbestos etc.
MAN – MADE FIBERS:
1. Regenerated Fibers – Viscose Rayon, Diacatate, Triacetate etc.
2. Synthetic Fibers – Nylon, Polyester, Acrylic, Polypropylene, Polyethylene etc.
3. Mineral Fibers – Glass, Steel, Carbon, Ceram etc.
READING MATERIAL -
Origin and Nature of Cotton Fiber
The cotton fibre is obtained from the cotton plant by the following processes:
1. Cultivation: Cotton is the oldest fiber and grown in warm and hot climate. The bowing
season of cotton in India is in the month of April and May. The seed of cotton is takes about 3
months to develop in a young plant. The flowers are converted into fruits which are known as cotton
balls. The cotton fibers are grown from skin of seed present in cotton balls. Finally the cotton balls
splits and the fibers are ready for harvesting by the month of September and October.
2. Harvesting: Harvesting of cotton fiber is done manually by hand picking in India whereas in
developed countries harvesting is done by machines. The harvested cotton fibers are then send to
ginning mills.
3. Ginning And Bailing: In ginning mills cotton fibers are separated from seeds. This process
is called ginning and it is carried out ginning machines. The cotton fibers are so obtained and then
packed in the forms of bales. This process is called bailing and it is done in bailing press. The
average bale weight is kept from 150 to 200 kg aprox.
Mature cotton has Bean or Kidney shaped cross section, and a small lumen. Immature cotton
also has a bean shaped cross section but a larger lumen. Mercerised cotton looksalmost round to
oval, a small point at or near the centre representing the lumen
Varieties of Cotton
1. Sea Island Cotton: It is the highest quality and also very costly cotton. It grows on the cost
of the gulf of Florida. The average length of this cotton is 2 inch and diameter is 1/1500 inch. This
cotton is used to making yarn up to 300 count.
2. Egyptian Cotton: There are two types of Egyptian cotton white cotton and brown cotton.
Average length is 1.5 inch and diameter is 1/1500 inch. It is suitable for up to 200 count.
3. South American Cotton: The average length of cotton is 1- 1.5 inch and diameter is 1/1300
inch. It is suitable for making yarn up to 150 count.
4. North American Cotton: Its average length is 1- 2.5 inch and diameter is 1/1200 inch. It is
suitable for yarn 70 count.
5. Indian Cotton: The average length of Indian cotton is 0.6 to 0.8 inch and diameter is 1/1200
inch. It is suitable for yarn up to 20.50 count.
6. China Cotton: The average length of cotton is 0.5 to 0.7 inch and average diameter is
1/1200 inch. It is suitable for yarn up to 20.50 count.
Syllabus - Origin, nature and appearance of Wool Fibre. Impurities in wool. Physical & chemical
properties of Wool Fibre. End use of Wool.
Origin, nature and appearance of Silk Fibre. Impurities in Silk. Physical & chemical properties of
Silk Fibre. End use of Silk
Origin, nature and appearance of Jute Fibre. Impurities in Jute. Physical & chemical properties of
Jute Fibre. End use of Jute
READING MATERIAL -
WOOL FIBER
Origin and Nature of Wool Fibre:
Wool is natural fibre obtained from animals like Sheep, Goat, Rabbit and Camel. It has protein in it.
Wool is formed by 18 aminoacids, distributed in a particular order. A polyamide is formed by this
which is called ‘keratein’ used for actual fiber forming material of Wool.
The wool fibre is obtained by the following processes:
1. Shearing – It is the process of taking the wool from the body of sheep by using hand
operated or machine operated cutters.
2. Sorting And Grading – Shorting and grading of wool is done before selling it to market by
skilled workers depending on the type, staple length, fineness and part of sheep body e.t.c. and
priced accordingly. The grading of wool is done according to the British numbering system
depending upon the yarn, which can be made from it. The grading of wool in United State is based
upon the superior quality obtained from Merino sheep e.g. Half-blood, Three-eigth-blood,
Quartered-blood, Low-quarter-blood, Common and Braid.
3. Scouring – The wool fiber contain a lot of impurities like grease, dust and dirt because the
sheep remains mostly in fields. So these impurities are removed in scouring process by treating with
mild alkaline solution. In scouring the wool fibers are passed through warm water, soap solution and
mild solution of soda ash. If wool fibers contain more impurities then they are passed through a
dilute solution of Hydrochloric acid.
4. Drying – After souring wool fibers are dried in sun light or with driers to eliminate moisture
present in fibers.
5. Oiling – In order to improve spinning performance the wool fibers are treated with some oils,
this process is known as oiling.
6. Dyeing – The wool fibers are dyed in the required shade if fiber dyed yarn is to be made.
7. Blending – The wool fibers may be blended with other fibers like cotton, polyester, acrylic
as required and then subjected to further spinning processe.
Appearance of Wool
Microscopic view
i. Longitudinal view:
In longitudinal view wool is irregular and roughly cylindrical. Scales are present on thesurface.
ii. Cross sectional view
It is oval shaped or circular shaped with variation in diameter.
iii. Morphological/ Structural view:
Physical structure of wool appears to be circular cylindrical that tapers from root to tip. From
microscopic or morphological point it has 4 parts.
a. Epicuticle, or Outer sheath: It is the outer most non-protein, thin and water repellent
covering. However, it has smallmicroscopic pores which help wool fiber fabrics to absorb water
vapors from human body, and release it into air.
b. Cuticle: These are scales like cells, which are present under the epicuticle as layers. These
layers are called epicuticle, exocuticle, endocuticle. These overlap and protrude for about one third
of their length, the ends being directed towards the tip of the fibre. The outer most layers of these
scales is a tough membrane known as the epicuticle. Beneath this the exocuticle is situated and the
innermost layer described as the endocuticle. These cause aspecial directional frictional effect that
has a very important influence on the frictional behavior of wool fibres.
c. Cortex: Bulk of fiber is made of cortical cells or cortex and is enclosed by the cuticle cells.
Theseare fibrils (macro and micro fibrils) present in the cortex. Wool is bilateral structure – ortho
and paracortex. The corticle cells are 100-200 µ in length and 2-5 µ wide. The tensile strength,
elastic properties and the natural colour of the wool are determined mainly by the nature of the
cortical cells.
d. Medulla:
There is a hollow space in the center running along the length of fiber. Many coarse wool fibres have
a hollow space in the centre. The Medulla is absent in fine wools.
Impurities in Wool:
The wool fibres contain approximately 61% keratin and around 39% impurities such as: Wax,
Grease, Suint, Dust, Dirt, Vegetable Particles etc.
Dirt is acquired by the animals (sheep, goat) while roaming.
Saint is an impurity due to sweating and in complex mixture soluble in water.
Fat is yellowish wax like substance and is made of fatty acids and cholesterol. It is soluble in
organic solvant. Wool scouring is done to remove this fat or wax with soap and soda ash.
Burrs, seed and straw are vegetable matters. They are removed mechanically or chemically
(carbonizing).
Carbonization is removal of seeds (cellulosic materials) by treatment with mineral acids.
Physical Properties of Wool Fiber
1. Length – varies from 1.5 inches to 15 inches. The width of wool fiber is 15 to 17 microns. It
has crimps or weaviness.
2. Luster- It has medium luster.
3. Strength- It strength lies between 1 to 1.7 grams per denier. Its decreases on wetting.
4. Enlongation- Its enlongation is 20% to 40%.
5. Elastic recovery – It has 99% elastic recovery.
6. Resiliency – It has excellent resiliency.
7. Density – It has density of 1.3 to 1.32 grams per cc (centimeter cube).
8. Moisture Regain – Its capacity for moisture regain is 13.5% to 16%.
SILK FIBER
Nature of Silk:
Silk is the only natural fibre that occurs in the form of a fine continuous filament which is produced
from the body fluid of silkworm.
In addition to the luster, strength is one of the most interesting characteristics of silk. At first touch,
one may feel that silk is fragile but it’s actually one of the strongest fibre.
Appearance of Silk:
Raw Silk strand consists of 2 Silk filaments encased by a protein called sericin. Raw silkhas uneven
and irregular surface due to sericin coating. Silk is a very fine regular translucent Microscopic View:
Nature of Jute
Jute fibre is a type of plant fibre which is widely known for its ability to be spun into strong and
coarse threads. Individual jute fibres are known to be soft, long, and shiny in nature. The jute fibre
yarn is widely used for ropes/ cords and the jute fabric is used for packaging material.
Appearance of Jute
Microscopic Structure
i. Longitudinal View:
Length wise Jute fibre shows irregular thickness (contrictions) in the cell wall.
Externally jute fibre is smooth with nodes.
ii. Cross-sectional View: Cross section is generally round or oval shaped but these
are polygonal structureswith sharp and defined angles.
Syllabus - Regenerated Fibers - Monomers of regenerated fibres. Sequence of steps for making
fibre. formula, physical & chemical properties Viscose rayon. End use of Viscose rayon. Monomers
of regenerated fibres Acetate rayon. Sequence of steps for making fibre. formula, physical &
chemical properties Acetate rayon. End use of Acetate rayon
READING MATERIAL -
4.1. Introduction
Regenerated fibres are manufactured from a natural polymer, cellulose, which is obtained from
wood. Cellulose is reacted chemically so as to make viscos solution which can be extruded to make
viscose fibres. These fibres are chemically similar to cotton and share their desirable properties of
moisture absorbancy. The first regenerated fibre, called rayon, which was originally intended to be a
substitute for silk.
By adopting the basic production process, a range of viscose fibres with different characteristics,
like high tenacity, high wet modulus, crimped and inflated fibres can be produced for different uses.
The viscose process is long and complicated and the byproducts give rise to environmental
problems. So other man-made cellulosic fibres are produced called modified re-generated fibres by
using an alternate process. These fibres include cellulose, diacetate and tri-acetate. The raw material
is cellulose, but in these fibres it is modified chemically so that polymer can be dissolved in an
organic solvent. These fibres are produced almost entirely as continuous filament yarns and are used
in soft silk like dress fabrics. Most cigarette filter tips are made from cellulose di-acetate fibres.
4.2. Viscose rayon
Viscose rayon is a regenerated cellulosic fibre and cellulose is the raw material for producing this
fibre. It is obtained by the process viscose. The name viscose was derived from the liquid state of the
spinning solution as the spinning solution is thick and flow like honey.
4.2.1. Manufacturing process
Flow diagram for production of viscose rayon filament and viscose fibre is givenas per following
Flow chart
Cellobiose is the basic unit of the cuprammonium, polynosic and viscose rayon.
Cellulose, in regenerated form, is the polymer of these three regenerated cellulose fibres; their
degree of polymerisation is about
• 250 cellobiose units (i.e. n = 250) for cuprammonium;
• 300 cellobiose units (i.e. n = 300) for polynosic;
• 175 cellobiose units (i.e. n = 175) for viscose.
The raw material for the viscose rayon is cellulose (Cellulose is a white amorphous, shapeless
substance that forms the cell walls of plant life. Chemically, it is a carbohydrate. Carbohydrate is a
compound, sugar, starch or cellulose of carbon with hydrogen and oxygen). Viscose rayon is
obtained by reduction of cotton linters or high alpha cellulose woods to a pulp, same as in the
manufacture of paper. The pulp is bleached and pressed into sheets this is done in the pulp mill. In
the rayon mill the following are the processes to manufacture the rayon filament or fibre.
Steeping
Shredding
Ageing
Xanthation
Dissolution
Filtration
Blending
Ripening
Wet Spinning
(a) Steeping
The cellulose sheets are soaked in alkali in the steeping tank containing 17-18% NaOH for 30-60
minutes at temperature 18°C. After steeping, sheets of cellulose are pressed to remove the excess
alkali.
(b) Shredding
In this operation the cellulose sheets are shredded mechanically into fluffy crumbs. At this stage
surfactants like polyethylene glycol are added to decrease the surface tension and improve
dispersion of carbon disulphide during the later process of xanthation.
(c) Ageing
This is depolymerisation step in the presence of oxygen. Here the degree of polymerization come
down from 1000 to 300. In this process the crumbs are stored in rectangular galvanized steel
container covered with lids. The oxygen present within the crumbs is responsible for the
depolymerisatioin, exposure to outside air is avoided. Aging is carried out for 24-72 hours at 25-
30°C. The process can be accelerated in the presence of catalysts or at higher temperature.
(d) Xanthation
The aged alkali is transferred into sealed hexagonal drums rotating at 2-4 revolutions per minute
where the 10 % by weight of cellulose carbon disulphide is introduced. The process is carried out for
2-4 hrs and the colour change takes place from white to yellow, yellow to deep yellow and then to
reddish orange. The product at this stage is sodium cellulose xanthate in the form of small balls.
(e) Dissolution
Dissolution of sodium cellulose xanthate is carried out in 4 - 6% solution of NaOH in a cylindrical
vessel provided with agitators for 4 - 5 hours. The air whipped into the solution is removed by
evacuation.
(f) Filtration
The solution is filtered to remove any impurities and un-dissolved cellulosic particles. Filtration is
done at several stages.
(g) Blending
To have the uniformity and to avoid any batch to batch variation, viscose solutions from several
tanks are mixed in a large vessel.
(h) Ripening
The viscose solution obtained is difficult to coagulate. The solution is kept for 1 - 3 days for
ripening, at this stage the solution is kept at controlled temperature 15 - 25° C. In this step various
changes takes place, here first the degree of polymerization falls and then rises to original value. The
ripened solution is again filtered carefully to remove any foreign matter and deaerated. Pigments can
be added to produce died fibres. Delustering agents TiO2 is added for controlling the lustre and
other chemicals for special yarns. After ripening the solution is ready for spinning.
(i) Wet spinning
In the spinning of the solution into fibre formation, the regeneration of cellulose from cellulose
xanthate in the presence of acid takes place. Spinning is carried out by extrusion of the spinning
solution from the spinneret having the tiny holes (diameter is in the order of 0.05 mm). Spinneret is
present in the coagulation bath. The spinning speed may be as high as 120 m/min. As the acid in the
coagulation bath diffuse into the filaments, regeneration of the cellulose takes place. The
composition of the coagulation bath is as follows
H2SO4 - 8 - 10 %
Na2SO4 - 16 - 24 %
Glucose - 2%
ZnSO4 - 1 - 2%
H2O - 69 %
Each chemical has its own function; Na2SO4 precipitates the sodium cellulose xenthate from the
viscose solution into filaments and H2SO4 converts in to cellulose, Glucose gives the pliability and
softness to the filaments and ZnSO4 is responsible for added strength and serrated cross section.
(j) Winding and stretching
Winding the stretching of the filaments is also done to orient the molecules in the direction of the
fibre axis to improve the mechanical properties of the filaments. After that the filaments strands are
wound and are further processed with following operations.
Washing
Desulphurising
Bleaching
Washing
Drying
Winding
The cake is washed with water to remove the impurities using a cake washing machine. After that it
is washed with sodium sulphide solution at 62 65°C to remove the residual sulphur. Then bleaching
is done with sodium hypochlorite or with hydrogen per-oxide (H2O2) to remove the residual
chlorine, cake is treated with mild HCl in the case of sodium hypochlorite bleaching and finally it is
dried.
4.2.2. Properties
(A) Physical properties
(i) Degree of - 175 - 240 celluboise
polymerization
(ii) Amorphous region- 60 – 65%
(iii) Crystalline region - 35 – 40%.
(iv) Moisture regain - 11-12 %
(v) Tenacity - 14 – 45 g/tex (dry)
50% of the dry (wet)
(vi) Specific gravity - 1.49 g/cm3
(B) Chemical properties
Chemical properties of the viscose rayon are similar to cotton being cellulosic fibre. Shorter polymer
and very amorphous region are responsible for greater sensitivity to acids, alkalis, bleaches, sunlight
and weather in comparison to cotton.
4.2.3. Uses
The role of viscose rayon in the field of man-made fibres is similar to that of cotton in natural fibres.
Rayon is relatively cheap and has a wide range of applications. Its lustre is high but it can be
appropriately delustred. Viscose rayon conducts heat more readily than silk, the most lustrous
natural fibre, and rayon has a cooler feel against the skin. The loss of strength that viscose undergoes
under wet conditions can be controlled and brought to a minimum by modern resin finishes.
The introduction of rayond staple has opened prospects for blending rayon with other natural or
synthetic staple fibres and in fact, rayon staple is quite largely used in this fashion. Rayon imparts its
unique moisture absorption character and some other ‘cellulosic’ features to its blends with stronger,
lighter and less moisture absorbing fibres. Rayon-cotton, rayon-polyester, rayon-jute and rayon-
wool blends made by using rayons of appropriately matching staple lengths are of particular
importance.
Cellulose acetate
4.3.1. Introduction
The three types of rayon- viscose, cuprammonium and nitro-cellulose are known as regenerated
rayons since the original raw material, cellulose, is changed chemically in to another form, which in
turn is again changed i.e. again regenerated into cellulose once more. The forth method i.e. cellulose
acetate is not a regenerated cellulose product, as the filaments are not regenerated cellulose, but are
formed from cellulose acetate which is a derivative of cellulose.
4.3.2 Polymer system
The hydroxyl groups on the cellulose polymer are acetylated to the degree that the acetate or
secondary cellulose acetate polymer has less than 92 per cent but at least 74 per cent of its hydroxyl
groups acetylated; that is, 2.3 to 2.4 of the OH-groups per glucose unit are acetylated. This is usually
shown as 4 acetate groups per cellobiose unit.
The acetate or secondary cellulose acetate polymer, DP is about 130 units i.e. n = 130
The triacetate or primary cellulose acetate polymer has at least 92 per cent of its hydroxyl groups
acetylated. In general, this is shown as 6 acetate groups per cellubiose unit [Fig. 3.4 (b)].
The triacetate or primary cellulose acetate polymer, DP is about 225 units i.e. n = 225
The flow diagram for the manufacture of cellulose acetate rayon is as
Raw material
Purification
Pretreatment
Acetylation
Hydrolysis
Spinning
(a) Raw material: The raw material for cellulose acetate is cotton linters or wood pulp.
(b) Purification: First cotton linters are purified by kier boiling under pressure for 4-10 hours
followed by washing and then bleaching with sodium hypochlorite and drying.
(c) Pretreatment: The purified cotton is steeped in glacial acetic acid under controlled temperature to
make it more reactive
(d) Acetylation: In this process the cotton is treated with an excess of acetic anhydride and glacial
acetic acid in an closed vessel fitted with a powerful stirrer. H 2SO4 increases the rate of reaction.
Reaction is exothermic and the vessel is cooled to keep the temperature low otherwise degradation
of cellulose takes place. For the first four hours the temp. is kept at 20°C and then increased to 25-
30°C for the next 7-8 hours. The cellulose dissolves completely in to the reaction mixture then it is
considered to be completely acetylated. At this stage all the three hydroxyl groups of the cellulose
are replaced by three acetyl groups. This is also called cellulose triacetate or primary acetate.
(e) Hydrolysis: Primary acetate is not suitable for spinning as it is soluble only in expensive and
objectionable solvent chloroform. The hydrolysis of primary acetate is done to convert it into
acetone (cheap) soluble called secondary acetate or diacetate. In this step the primary acetate is run
into water with excess acetic acid anhydride (95 % solution of acetic acid in water) for 20 hours at
high temperature. During this hydrolysis of cellulose triacetate takes place and some of acetyl
groups are replaced by hydroxyl groups. Degree of acetylation in the secondary or diacetate is about
2.3. Degree of polymerization is in the range of 350-400. The cellulose diacetate is washed
separately centrifuged and dried at low temperature. Blending of various batches is carried out for
uniformity and to reduce the batch to batch variation.
(f) Preparation of spinning solution: The spinning solution 25-35 % is prepared with acetone in a
closed vessel. For completely dissolution it takes around 24 hours. Dulling agents, like TiO 2 and
other coloring pigments are added at this stage if required. The spinning solution is called Dope. The
dope is filtered and deaerated.
(g) Spinning: The dope is extruded through the spinnerets having tiny holes located inside of the
spinning cabinet. In the cabinet hot air at temp 100°C is circulated form the bottom, this causes the
evaporation of acetone. The air with the acetone is allowed to escape the cabinet from the top and is
taken to recovery plant from where the acetone is recovered and reused. The hardened filaments
move down to feed rollers.
Stretch is applied on the filaments to orient the molecules in the direction of applied force to
improve the mechanical properties of the filaments and are finally wound upon the bobbins
individually or in filaments form. Several spinneretes are drawn together in the form of the rope
called Tow. For the manufacture of staple fibres, after drawing process crimping is carried out and
then the fibres are cut into desired length that may be used as alone or blended with other fibres.
4.3.3. Properties of cellulose acetate
(A) Physical properties
(i) Degree of polymerization 130 - 225 celluboise
(ii) Amorphous region 60 %
(iii) Crystalline region 40%.
(iv) Moisture regain 6.5 %
(v) Tenacity 1.2 g/tex (dry)
(vi) Specific gravity
Triacetate 1.32 g/cm3
Acetate 1.25 - 1.30g/cm3
(B) Chemical properties
Chemical properties of the acetate rayon are similar to cotton being cellulose “back bone” fibre.
Shorter polymer and very amorphous region are responsible for greater sensitivity to acids, alkalis,
bleaches, sunlight and weather in comparison to cotton.
Burning test
Cellulose acetate rayon will melt when placed close to flame, the residue is hard, blackish-brown
bead, difficult to crush between the fingers.
4.3.4. Uses
Drip-dry property, permanent pleating effect and ‘need no-ironing’ character of the triacetate make
it a good choice for easy-care slacks, skirts and dresses. In the staple form, it is suitable as a blend
component with other staple fibres, such as cotton and viscose, needing moderately high ironing
temperature due to its relatively high melting temperature. Blended with wool, the triacetate
provides fabrics having the characteristic heat-setting and drip-dry properties combined with the
warmth of wool.
ACRYLIC
Acrylic fibre is synthesised through polymerisation of acrylonitrile (vinyl cyanide) and has the
chemical name polyacrylonitrile (PAN) with the empirical formula where 'n' is the degree of
polymerisation. Acrylic fibers are made by spinning acrylonitrile copolymers containing at least
85% acrylonitrile monomer. Typical comonomers are vinyl acetate or methyl acrylate To produce
continuous filaments, the polymer is dissolved in a solvent and extruded through spinnerets.
Afterwards, the continuous filaments are washed and dried.
General Properties
Absorbency Poor
Elasticity Good
POLYESTER FIBRE
Polyester is a synthetic fiber, but its raw materials still come from nature. Most polyester is made
out of petroleum, a natural non-renewable resource.
The chemical name of polyester is Polyethylene terephthalate the polyester with the greatest market
share, is a synthetic polymer made of purified terephthalic acid (PTA) or its dimethyl ester dimethyl
terephthalate (DMT) and monoethylene glycol (MEG).
NYLON 6
Nylon-6 is manufactured from the monomer called caprolactum. The monomer caprolactum is
heated at 533 K in an inert atmosphere, it polymerises to give nylon-6.
Caprolactum has 6 carbons hence called Nylon 6
Nylon 6 has certain advantages over Nylon 6,6,. Firstly the systheisi fo caprolectum is easier than
that of Hexamethylene Diamine and Adipic Acid. Therefore it is cheaper to make Nylon 6 than
Nylon6,6. Secondly Nylon 6 has greater affinity for acid dyes than Nylon6,6,
Physical Properties of Nylon 6
1. Density: 1.14 g/cc
2. Tenacity: Dry= 4.2-5.8 gpd, Wet=4.0-5.3 gpd
3. Elongation at Break--> Dry = 24-40, Wet=28-43
4. Elastic Recovery at 4% extension= 100%
5. Moisture Regain= 4%
6. Because of low MR, wet nylon dries quickly.
7. Melting Point= 215 deg C ( Nylon 66-250 deg C)
8. It is weakened by prolonged exposure to sunlight.
Uses of Nylon 6
1. Tyre Cord Manufacturing
2. Fishing Lines
3. Luxury Yachts
4. Stockings with good fit, sheerness, quick washing and drying properties.
NYLON 66
Nylon-6,6 is a polymer formed by the polymerization reaction of hexamethylenediamine and adipic
acid. Thus, the monomers of nylon-6,6 are of hexamethylenediamine and adipic acid.
SPANDEX/ LYCRA
Both Lycra and Spandex are the same. Spandex is the generic name of fiber and Lycra is a
spandex product of DuPont company. When you are specifically using Lycra® product (spandex
fiber) for your clothing products,
What is Spandex?
Spandex is a synthetic polymer. It is also called Elastane Fiber. Chemically, it is made up of a long-
chain polyglycol combined with a short di-isocyanate, and contains at least 85% polyurethane. It is
an elastomer, which means it can be stretched to a certain degree and it recoils when released. These
fibers are superior to rubber because they are stronger, lighter, and more versatile. In fact, spandex
fibers can be stretched to almost 500% of their length.
Molecular Structure:
Spandex is a polymer; its macromolecular structure is made up of repeating units (mars) denoted by
the x and n next to the parentheses in the structure. Each Spandex fiber will differ somewhat in
length and composition depending on the exact value of x and n.
Fig: Chemical
Structure of spandex
Microscopic view of spandex is-