Manufacturing of Manmade Fibers / Synthetic Fibers
Manmade fibers are manufactured using different mechanical and chemical
processes for example Synthetic fibers from thermoplastics are produced
by extruding the molten plastic through extrusion dies (spinnerets) into
a stream of cold air that cools and solidifies the plastic. (The
operation is referred to as melt spinning.)
General Principles of Production Process
Polymerisation
The term polymerization defines the process of macromolecules formation
through repetition of basic units: it, of course, applies only to
synthesis fibers. In general, polymerization reactions are activated and
controlled during the process by various parameters, as temperature,
pressure,
catalyzers, reaction stabilizers.
catalyzers, reaction stabilizers.
The number of repetitive units is termed degree of polymerization and is
a parameter of great significance for fiber properties setting. As the
length of the single molecules is not constant but varies according to a
statistical model, the degree of polymerization or the correspondent
molecular weight has to be considered as an average value.
Depending on the various fiber typologies, the degrees of polymerization
may range from some hundred units in the case of polymers obtained
through condensation (PA, PES) to some thousand units in the case of
polymers resulting from poly-addition (PAN, PP). Under a production and
application point of view, the degree of polymerization is controlled by
measuring following parameters:
- Relative viscosity rel= solution viscosity/solvent viscosity = flow time t1/flow time t2
- Intrinsic viscosity intr= rel /c ?0 (concentration vanishing)
- Melt flow index MFI = speed rate of the melted polymer at pre-established conditions
Relative viscosity is a parameter which is mostly used to identify
nylon, while intrinsic viscosity (obtainable from the relative viscosity
also by means of formulas) is used for polyester and the melt flow
index for polypropylene.
There are basically two mechanisms of chemical reaction available for the synthesis of linear polymers:
- Poly-condensation: with this operation two molecules of the same type or of different types are joined together to form macromolecules by removing simple secondary products as water, hydrochloric acid, alcohol. The prerequisite for reactions of this type is the presence in the molecule (monomer) of two terminal reactive groups with functional properties.
- Poly-addition: this operation joins together several molecules and redistributes the valence links existing in the monomers, however without removing secondary products.
Many unsaturated compounds which are characterized by the presence of a double link between
two adjacent carbon atoms as ethylene and its derivatives polymerise according to this reaction;
within this category fall e.g. acrylic and polyolefin fibers.
two adjacent carbon atoms as ethylene and its derivatives polymerise according to this reaction;
within this category fall e.g. acrylic and polyolefin fibers.
Spinning
The term spinning defines the extrusion process through bored devices
(spinnerets) of fluid polymer masses which are able to solidify in a
continuous flow. The spinning process is sometimes designated as
“chemical or primary spinning” to distinguish it from the “textile or
mechanical or secondary spinning”. The polymer processing from the solid
to the fluid state can take place with two methods:
by melting:
this method can be applied on thermoplastic polymers which show stable
performances at the processing temperatures (this method is used by 70%
of the fibers)
by solution:
the polymer is solved in variable concentrations according to the kind
of polymer and of solvent, anyhow such as to produce a sufficiently
viscous liquid (dope) (this method is used by 30% of the fibers)
Solvent removal can take place in two ways:
Dry spinning
The solvent is removed through flows of warm gas suitably directed to
the extruded filaments; gas temperature should be higher than the
boiling temperature of the solvent, which will be extracted from the
filaments, recovered and recycled. Filament solidification proceeds
according to the extent of solvent evaporation; it takes place faster on
the external yarn layers (thus creating a crust or skin), and
successively slows down while proceeding towards the interior. As a
consequence of the mass exchange, the original (round) cross-section of
the filament undergoes a contraction, thus generating cross-sections
which characterize the various kinds of fibers and spinning processes.
Wet spinning
This spinning method is based on the introduction of an extruded
polymeric viscose into coagulation baths where the liquor, usually
water, behaves as a solvent towards the polymer solvent and as a
non-solvent towards the polymer mass.
Practically the solvent which is contained in the fiber in the amorphous
state (gel) is spread towards the liquor and at the same time, the
liquid of the bath is spread towards the interior of the fiber. The
processing speeds are dependent on several parameters, as type and
concentration of the
polymeric solvent and of the liquor, which bring about structural variations in the fiber. In particular the formation of an outer gardened and more compact cortex (skin), similarly to what happens in dry spinning, slows down the coagulation mechanism of the inner filament portion (core), thus creating unevenness with a more or less porous structure (voids formation). The fiber cross-sections result more or less modified, from the original round form to a lobated form, with a wrinkled surface.
polymeric solvent and of the liquor, which bring about structural variations in the fiber. In particular the formation of an outer gardened and more compact cortex (skin), similarly to what happens in dry spinning, slows down the coagulation mechanism of the inner filament portion (core), thus creating unevenness with a more or less porous structure (voids formation). The fiber cross-sections result more or less modified, from the original round form to a lobated form, with a wrinkled surface.
Drawing
The polymer extruded by the spinnerets in form of filaments has not yet
the properties which are typical of a textile fibre: in fact the polymer
mass (solidified through cooling or solvent removal) is characterized
by a mass of disorderly placed molecular chains (in amorphous state)
which provides the material with poor thermal and chemical stability,
low resistance to ageing, high plasticity and deformability and
consequently insufficient physical/textile properties. If we take
natural fibers as models, we need to orientate the molecular chains
(orientation phase) in the direction of the fiber axis and at the same
time or successively activate or increase the ordered arrangement of the
intermolecular structure (crystallization phase).
Continuous filament yarns
Continuous filament yarns can be composed of a single filament
(monofilament yarns) or of several filaments (multifilament yarns) and
are described through abbreviations, the first figure of which indicates
the total linear mass (expressed in dtex or, less usually, in den), the
second figure indicates the filament number and a third figure if any
shows the twists per length unit (turns/m) imparted to the yarn.
Monofilaments for traditional textile uses have linear masses ranging
from 10 to 50 dtex approximately; monofilaments with larger linear
masses find on the contrary use in technical applications and are
identified with their thickness expressed by the diameter of the round
cross-section (0.06?2 mm).
General principles of manmade fiber manufacturing
There is no substantial difference in the structure of natural fibers
from that of man-made Fibres: both fiber categories are composed of
macromolecules or by linear polymers, that is by the repetition of
several simple molecules (monomers).
Man-made fibers are fibers in which either the basic chemical units have
been formed by chemical synthesis followed by fiber formation or the
polymers from natural sources have been dissolved and regenerated after
passage through a spinneret to form fibers. Those fibers made by
chemical synthesis are often called synthetic fibers, while fibers
regenerated from natural polymer sources are called regenerated fibers
or natural polymer fibers. In other words, all synthetic fibers and
regenerated fibers are man-made fibers, since man is involved in the
actual fiber formation process.
Natural fibers are essentially composed of atoms of various elements,
such as carbon, hydrogen, oxygen, sometimes of nitrogen and other
elements (sulphur) in lower quantities; during their biological growth,
these elements form the rings of long molecular chains. The development
of man-made fibres was based on the knowledge acquired with natural
fibers which structure was taken as a model; the difference between the
two fiber categories is that natural fibres form macromolecules through
biological growth, while the growth process of man-made fibres is driven
by technical equipment (artificial fibers use instead of natural
polymers).
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