Aramid Fiber Uses

  • Flame-resistant clothing
  • Heat protective clothing and helmets
  • Body armor, competing with PE based fiber products such as Dyneema and Spectra
  • Composite materials
  • Asbestos replacement (e.g. braking pads)
  • Hot air filtration fabrics
  • Tires, newly as Sulfron (sulfur modified Twaron)
  • Mechanical rubber goods reinforcement
  • Ropes and cables
  • Wicks for fire dancing

Aramid fiber characteristics

  • Good resistance to abrasion
  • Good resistance to organic solvents
  • Nonconductive
  • No melting point, degradation starts from 500°C
  • Low flammability
  • Good fabric integrity at elevated temperatures
  • Sensitive to acids and salts
  • Sensitive to ultraviolet radiation
  • Prone to static build-up unless finished

overview of Aramid Fiber

Aramid fibers are a class of heat-resistant and strong synthetic fibers. They are used in aerospace and military applications, for ballistic rated body armor fabric, and as an asbestos substitute. The name is a shortened form of "aromatic polyamide". They are fibers in which the chain molecules are highly oriented along the fiber axis, so the strength of the chemical bond can be exploited.

Appearances of Aramid Fiber Characteristics
Fiber,Chopped fiber,Powder, Pulp

Acrylic Fiber Uses

Apparel: Sweaters, socks, fleece wear, circular knit apparel, sportswear and childrens wear 
 
Home Furnishings: Blankets, area rugs, upholstery, pile; luggage, awnings, outdoor furniture 
 
Other Uses: Craft yarns, sail cover cloth, wipe cloths 
 
Industrial Uses: Asbestos replacement; concrete and stucco reinforcement

Acrylic Fiber Characteristics

  • Outstanding wickability & quick drying to move moisture from body surface
  • Flexible aesthetics for wool-like, cotton-like, or blended appearance
  • Easily washed, retains shape
  • Resistant to moths, oil, and chemicals
  • Dyeable to bright shades with excellent fastness
  • Superior resistance to sunlight degradation

Basic Principles of Acrylic Fiber Production

Acrylic fibers are produced from acrylonitrile, a petrochemical. The acrylonitrile is usually combined with small amounts of other chemicals to improve the ability of the resulting fiber to absorb dyes. Some acrylic fibers are dry spun and others are wet spun. Acrylic fibers are used in staple or tow form.

Spandex Fiber Characteristics

  • Can be stretched repeatedly and still recover to very near its original length and shape
  • Generally, can be stretched more than 500% without breaking
  • Stronger, more durable and higher retractive force than rubber
  • Lightweight, soft, smooth, supple
  • In garments, provides a combination of comfort and fit, prevents bagging and sagging
  • Heat-settable - facilitates transforming puckered fabrics into flat fabrics, or flat fabrics into permanent rounded shapes
  • Dyeable

Major spandex fiber uses

Apparel and clothing articles where stretch is desired, generally for comfort and fit, such as:
athletic, aerobic, and exercise apparel
wetsuitss
wimsuits/bathing suits
competitive swimwear
netball bodysuits
brassiere straps and bra side panels
ski pants
disco jeanss
lacks
hosiery
leggings
socks
diapers
skinny jeans
belts
underwear
dance belts worn by male ballet dancers and others
Compression garments such as:
surgical hose
support hose
cycling shorts
wrestling singlet
one piece rowing suits
foundation garments
motion capture suits
Shaped garments such as
bra cups
Home furnishings, such as microbead pillows

Spandex Fiber Production

Spandex-or elastane-is a synthetic fiber known for its exceptional elasticity. It is stronger and more durable than rubber, its major non-synthetic competitor. It was invented in 1959 by DuPont chemist Joseph Shivers. When first introduced, it revolutionized many areas of the clothing industry.
"Spandex" is a generic name and not derived from the chemical name of the fiber, as are most manufactured fibers, but an extension of the word expand. "Spandex" is the preferred name in North America; elsewhere it is referred to as "elastane".

Spandex fiber production

Spandex fibers are produced in four different ways, including melt extrusion, reaction spinning, solution dry spinning, and solution wet spinning. All of these methods include the initial step of reacting monomers to produce a prepolymer. Once the prepolymer is formed, it is reacted further in various ways and drawn out to produce a long fiber. The solution dry spinning method is used to produce over 90% of the world's spandex fibers.
 

Solution dry spinning

  • Step 1: The first step is to produce the prepolymer. This is done by mixing a macroglycol with a diisocyanate monomer. The two compounds are mixed together in a reaction vessel to produce a prepolymer. A typical ratio of glycol to diisocyanate is 1:2.
  •  
  • Step 2: The prepolymer is further reacted with an equal amount of diamine. This reaction is known as chain extension reaction. The resulting solution is diluted with a solvent to produce the spinning solution. The solvent helps make the solution thinner and more easily handled, and then it can be pumped into the fiber production cell.
  •  
  • Step 3: The spinning solution is pumped into a cylindrical spinning cell where it is cured and converted into fibers. In this cell, the polymer solution is forced through a metal plate called a spinneret. This causes the solution to be aligned in strands of liquid polymer. As the strands pass through the cell, they are heated in the presence of a nitrogen and solvent gas. This process causes the liquid polymer to react chemically and form solid strands. 
  •  
  • Step 4: As the fibers exit the cell, an amount of solid strands are bundled together to produce the desired thickness. Each fiber of spandex is made up of many smaller individual fibers that adhere to one another due to the natural stickiness of their surface.
  •  
  • Step 5: The resulting fibers are then treated with a finishing agent which can be magnesium stearate or another polymer. This treatment prevents the fibers' sticking together and aids in textile manufacture. The fibers are then transferred through a series of rollers onto a spool.
  •  
  • Step 6: When the spools are filled with fiber, they are put into final packaging and shipped to textile manufacturers
  • Characteristics of Nylon

    Variation of luster: nylon has the ability to be very lustrous, semilustrous or dull.
    * Durability: its high tenacity fibers are used for seatbelts, tire cords, ballistic cloth and other uses.
    * High elongation
    * Excellent abrasion resistance
    * Highly resilient (nylon fabrics are heat-set)
    * Paved the way for easy-care garments
    * High resistance to: insects, fungi and animals,molds, mildew, rot,many chemicals
    * Used in carpets and nylon stockings
    * Melts instead of burning
    * Used in many military applications

    Overview of Nylon Fiber

    Nylon is a generic designation for a family of synthetic polymers known generically as polyamides and first produced on February 28, 1935 by Wallace Carothers at DuPont. Nylon is one of the most commonly used polymers

    Density - 1.15g/cm³
    Electrical conductivity (σ) - 10-12S/m
    Thermal conductivity 0.25W/(m·K), 463 K-624 K
    Melting point 190°C-350°C or 374°F-663°F

    Nylon is a thermoplastic silky material, first used commercially in a nylon-bristled toothbrush (1938), followed more famously by women's stockings ("nylons"; 1940). It is made of repeating units linked by peptide bonds (another name for amide bonds) and is frequently referred to as polyamide (PA). Nylon was the first commercially successful synthetic polymer. There are two common methods of making nylon for fiber applications. In one approach, molecules with an acid (COOH) group on each end are reacted with molecules containing amine (NH2) groups on each end. The resulting nylon is named on the basis of the number of carbon atoms separating the two acid groups and the two amines. These are formed into monomers of intermediate molecular weight, which are then reacted to form long polymer chains.

    was intended to be a synthetic replacement for silk and substituted for it in many different products after silk became scarce during World War II. It replaced silk in military applications such as parachutes and flak vests, and was used in many types of vehicle tires.

    Nylon fibers are used in many applications, including fabrics, bridal veils, carpets, musical strings, and rope.

    Solid nylon is used for mechanical parts such as machine screws, gears and other low- to medium-stress components previously cast in metal. Engineering-grade nylon is processed by extrusion, casting, and injection molding. Solid nylon is used in hair combs. Type 6/6 Nylon 101 is the most common commercial grade of nylon, and Nylon 6 is the most common commercial grade of molded nylon. Nylon is available in glass-filled variants which increase structural and impact strength and rigidity, and molybdenum sulfide-filled variants which increase lubricity.

    Nylon Fiber production

    The first approach:

    * combining molecules with an acid (COOH) group on each end are reacted with two chemicals that contain amine (NH2) groups on each end.

    This process creates nylon 6,6, made of hexamethylene diamine with six carbon atoms and acidipic acid, as well as six carbon atoms.

    The second approach:

    * a compound has an acid at one end and an amine at the other and is polymerized to form a chain with repeating units of (-NH-[CH2]n-CO-)x.
    * In other words, nylon 6 is made from a single six-carbon substance called caprolactam.
    * In this equation, if n=5, then nylon 6 is the assigned name. (may also be referred to as polymer)

    Nylon 6,6

    * Pleats and creases can be heat-set at higher temperatures
    * Nylon 6 is very easy to dye, but Nylon 6,6 is not

    Nylon 6

    * Better dye Affinity
    * Softer Hand

    Polyester Manufacturing Process

    Fibre Manufacturing Process

    Today over 70 to 75% of polyester is produced by CP( continuous polymerisation) process using PTA(purified Terephthalic Acid) and MEG. The old process is called Batch process using DMT( Dimethy Terephthalate) and MEG( Mono Ethylene Glycol). Catalysts like 5b3O3 (ANTIMONY TRIOXIDE) are used to start and control the reaction. TiO2 (Titanium di oxide) is added to make the polyester fibre / filament dull. Spin finishes are added at melt spinning and draw machine to provide static protection and have cohesion and certain frictional properties to enable fibre get processed through textile spinning machinery without any problem.

    Polymerisation

    PTA which is a white powder is fed by a screw conveyor into hot MEG to dissolve it. Then catalysts and TiO 2 are added. After that Esterification takes place at high temperature. Then monomer is formed . Polymerisation is carried out at high temperature (290 to 300 degree centigrade) and in almost total vacuum. Monomer gets polymerised into the final product, PET (Poly ethylene Terephthalate).
     

    Melt Spinning

    This is in the form of thick viscous liquid. This liquid is them pumped to melt spinning machines. These machines may be single sided or double sided and can have 36/48/64 spinning positions. At each position , the polymer is pumped by a metering pump-which discharges an accurate quantity of polymer per revolution ( to control the denier of the fibre) through a pack which has sand or stainless steel particles as filter media and a spinnerette which could be circular or rectangular and will have a specific number of holes depending on the technology used and the final denier being produced. Polymer comes out of each hole of the spinnerette and is instantly solidified by the flow of cool dry air. This process is called quenching. The filaments from each spinnerette are collected together to form a small ribbon, passed over a wheel which rotates in a bath of spin finish: and this ribbon is then mixed with ribbon coming from other spinning positions, this combined ribbon is a tow and is coiled in cans. The material is called undrawn TOW and has no textile properties.

    Drawing and Cutting

  • At the next machine ( the draw machine), undrawn tows from severl cans are collected in the form of a sheet and passed through a trough of hot water to raise the temperature of polymer to 70 degrees C which is the glass transition temperature of this polymer so that the polymer can be drawn. In the next two zones, the polymer is drawn approximately 4 times and the actual draw or the pull takes place either in a steam chamber or in a hot water trough. After the drawing is complete, each filament has the required denier, and has all its sub microscopic chains aligned parallel to the fibre axis, thereby improving the crystallinity of the fibre structure and imparting certain strength.
  • The Future of Rayon

    The future of rayon is bright. Not only is there a growing demand for rayon worldwide, but there are many new technologies that promise to make rayon even better and cheaper.
    For a while in the 1970s there was a trend in the clothing industry toward purely synthetic materials like polyester. However, since purely synthetic material does not "breath" like natural material, these products were not well received by the consumer. Today there is a strong trend toward blended fabrics. Blends offer the best of both worlds. With the present body of knowledge about the structure and chemical reactivity of cellulose, some scientist believe it may soon be possible to produce the cellulose molecule directly from sunlight, water and carbon dioxide. If this technique proves to be cost effective, such hydroponic factories could represent a giant step forward in the quest to provide the raw materials necessary to meet the world wide demand for man-made fabric.

    Byproducts of Rayon

    As one of the industry's major problems, the chemical by-products of rayon have received much attention in these environmentally conscious times. The most popular method of production, the viscose method, generates undesirable water and air emissions. Of particular concern is the emission of zinc and hydrogen sulfide.
    At present, producers are trying a number of techniques to reduce pollution. Some of the techniques being used are the recovery of zinc by ion-exchange, crystallization, and the use of a more purified cellulose. Also, the use of absorption and chemical scrubbing is proving to be helpful in reducing undesirable emissions of gas.

    Quality Control in Rayon Manufacturing

    with most chemically oriented processes, quality control is crucial to the successful manufacture of rayon. Chemical make-up, timing and temperature are essential factors that must be monitored and controlled in order to produce the desired result.

    The percentages of the various fibers used in a blended fabric must be controlled to stay within in the legal bounds of the Textile Fiber Identification Act. This act legally defines seventeen groups of man-made fibers. Six of these seventeen groups are made from natural material. They include rayon, acetate, glass fiber, metallics, rubber, and azion. The remaining eleven fabrics are synthesized solely from chemical compounds. They are nylon, polyester, acrylic, modacrylic, olefin, spandex, anidex, saran, vinal, vinyon, and nytril.

    Within each generic group there are brand names for fibers which are produced by different manufacturers. Private companies often seek patents on unique features and, as could be expected, attempt to maintain legal control over their competition.

    Specialty Rayons

    Flame Retardant Fibers

    Flame retardance is achieved by the adhesion of the correct flame- retardant chemical to viscose. Examples of additives are alkyl, aryl and halogenated alkyl or aryl phosphates, phosphazenes, phosphonates and polyphosphonates. Flame retardant rayons have the additives distributed uniformly through the interior of the fiber and this property is advantageous over flame retardant cotton fibers where the flame retardant concentrates at the surface of the fiber. 

    Super Absorbent Rayons

    This is being produced in order to obtain higher water retention capacity (although regular rayon retains as much as 100 % of its weight). These fibers are used in surgical nonwovens. These fibers are obtained by including water- holding polymers (such as sodium polyacrylate or sodium carboxy methyl cellulose) in the viscose prior to spinning, to get a water retention capacity in the range of 150 to 200 % of its weight. 

    Micro Denier Fibers

    Rayon fibers with deniers below 1.0 are now being developed and introduced into the market. These can be used to substantially improve fabric strength and absorbent properties.

    Cross Section Modification

    Modification in cross sectional shape of viscose rayon can be used to dramatically change the fibers' aesthetic and technical properties. One such product is Viloft, a flat cross sectional fiber sold in Europe, which gives a unique soft handle, pleasing drape and handle. Another modified cross section fiber called Fibre ML(multi limbed) has a very well defined trilobal shape. Fabrics made of these fibers have considerably enhanced absorbency, bulk, cover and wet rigidity all of which are suitable for usage as nonwovens . 

    Tencel Rayon

    Unlike viscose rayon, Tencel is produced by a straight solvation process. Wood pulp is dissolved in an amine oxide, which does not lead to undue degradation of the cellulose chains. The clear viscous solution is filtered and extruded into an aqueous bath, which precipitates the cellulose as fibers. This process does not involve any direct chemical reaction and the diluted amine oxide is purified and reused. This makes for a completely contained process fully compatible with all environmental regulations.
  • Lyocell
  •  
  • A new form of cellulosic fiber, Lyocell, is starting to find uses in the nonwovens industry. Lyocell is manufactured using a solvent spinning process, and is produced by only two companies -- Acordis and Lenzing AG. To produce Lyocell, wood cellulose is dissolved directly in n-methyl morpholine n-oxide at high temperature and pressure. The cellulose precipitates in fiber form as the solvent is diluted, and can then be purified and dried. The solvent is recovered and reused. Lyocell has all the advantages of rayon, and in many respects is superior. It has high strength in both dry and wet states, high absorbency, and can fibrillate under certain conditions. In addition, the closed-loop manufacturing process is far more environmentally friendly than that used to manufacture rayon, although it is also more costly.
  • Different Types Of Rayons

    Rayon fibers are engineered to possess a range of properties to meet the demands for a wide variety of end uses. Some of the important types of fibers are briefly described.

    High Wet Modulus Rayon

    These fibers have exceptionally high wet modulus of about 1 g/den and are used as parachute cords and other industrial uses. Fortisan fibers made by Celanese (saponified acetate) has also been used for the same purpose.
    Polynosic Rayon
     
    These fibers have a very high degree of orientation, achieved as a result of very high stretching (up to 300 %) during processing. They have a unique fibrillar structure, high dry and wet strength, low elongation (8 to 11 %), relatively low water retention and very high wet modulus. 
     
     

    Manufacturing of Cuprammonium Rayon

    produced by a solution of cellulosic material in cuprammonium hydroxide solution at low temperature in a nitrogen atmosphere, followed by extruding through a spinnerette into a sulphuric acid solution necessary to decompose cuprammonium complex to cellulose. This is a more expensive process than that of viscose rayon. Its fiber cross section is almost round.

    Properties Of Rayon

    Variations during spinning of viscose or during drawing of filaments provide a wide variety of fibers with a wide variety of properties. These include:
    • Fibers with thickness of 1.7 to 5.0dtex, particularly those between 1.7 and 3.3 dtex, dominate large scale production.
    • Tenacity ranges between 2.0 to 2.6 g/den when dry and 1.0 to 1.5 g/den when wet.
    • Wet strength of the fiber is of importance during its manufacturing and also in subsequent usage. Modifications in the production process have led to the problem of low wet strength being overcome.
    • Dry and wet tenacies extend over a range depending on the degree of polymerization and crystallinity. The higher the crystallinity and orientation of rayon, the lower is the drop in tenacity upon wetting.
    • Percentage elongation-at-break seems to vary from 10 to 30 % dry and 15 to 40 % wet. Elongation-at-break is seen to decrease with an increase in the degree of crystallinity and orientation of rayon.
    Rayon Fiber Characteristics

    • Highly absorbent
    • Soft and comfortable
    • Easy to dye
    • Drapes well
    The drawing process applied in spinning may be adjusted to produce rayon fibers of extra strength and reduced elongation. Such fibers are designated as high tenacity rayons, which have about twice the strength and two-third of the stretch of regular rayon. An intermediate grade, known as medium tenacity rayon, is also made. Its strength and stretch characteristics fall midway between those of high tenacity and regular rayon.

    Manufacturing of Viscose Rayon

    Raw Materials

    Regardless of the design or manufacturing process, the basic raw material for making rayon is cellulose. The major sources for natural cellulose are wood pulp-usually from pine, spruce, or hemlock trees-and
    To make rayon, sheets of purified cellulose are steeped in caustic soda, dried, shredded into crumbs, and then aged in metal containers for 2 to 3 days. The temperature and humidity in the metal containers are carefully controlled. After ageing, the crumbs are combined and churned with liquid carbon disulfide, which turns the mix into orange-colored crumbs known as sodium cellulose xanthate. The cellulose xanthate is bathed in caustic soda, resulting in a viscose solution that looks and feels much like honey.cotton linters. Cotton linters are residue fibers which cling to cotton seed after the ginning process.

    Strictly defined, rayon is a manufactured fiber composed of regenerated cellulose. The legal definition also includes manufactured fibers in which substitutes have not replaced more than 15 percent of the hydrogens.
    While the basic manufacturing process for all rayon is similar, this fabric can be engineered to perform a wide range of functions. Various factors in the manufacturing process can be altered to produce an array of designs. Differences in the raw material, the processing chemicals, fiber diameter, post treatments and blend ratios can be manipulated to produce a fiber that is customized for a specific application.
    Regular or viscose rayon is the most prevalent, versatile and successful type of rayon. It can be blended with man-made or natural fibers and made into fabrics of varying weight and texture. It is also highly absorbent, economical and comfortable to wear.

    The Manufacturing Process

    While there are many variations in the manufacturing process that exploit the versatility of the fiber, the following is a description of the procedure that is used in making regular or viscose rayon.
    Regardless of whether wood pulp or cotton linters are used, the basic raw material for making rayon must be processed in order to extract and purify the cellulose. The resulting sheets of white, purified cellulose are then treated to form regenerated cellulose filaments. In turn, these filaments are spun into yarns and eventually made into the desired fabric.
    The process of manufacturing viscose rayon consists of the following steps mentioned, in the order that they are carried out: (1) Steeping, (2) Pressing, (3) Shredding, (4) Aging, (5) Xanthation, (6) Dissolving, (7)Ripening, (8) Filtering, (9) Degassing, (10) Spinning, (11) Drawing, (12) Washing, (13) Cutting. The various steps involved in the process of manufacturing viscose are explained below.

    Steeping

    Cellulose pulp is immersed in 17-20% aqueous sodium hydroxide (NaOH) at a temperature in the range of 18 to 25°C in order to swell the cellulose fibers and to convert cellulose to alkali cellulose.
    (C6H10O5)n + nNaOH ---> (C6H9O4ONa)n + nH2O

    Pressing

    The swollen alkali cellulose mass is pressed to a wet weight equivalent of 2.5 to 3.0 times the original pulp weight to obtain an accurate ratio of alkali to cellulose.

    Shredding

    The pressed alkali cellulose is shredded mechanically to yield finely divided, fluffy particles called "crumbs". This step provides increased surface area of the alkali cellulose, thereby increasing its ability to react in the steps that follow.

    Aging

    The alkali cellulose is aged under controlled conditions of time and temperature (between 18 and 30 C) in order to depolymerize the cellulose to the desired degree of polymerization. In this step the average molecular weight of the original pulp is reduced by a factor of two to three. Reduction of the cellulose is done to get a viscose solution of right viscosity and cellulose concentration.

    Xanthation

    In this step the aged alkali cellulose crumbs are placed in vats and are allowed to react with carbon disulphide under controlled temperature (20 to 30°C) to form cellulose xanthate.
    (C6H9O4ONa)n + nCS2 ----> (C6H9O4O-SC-SNa)n

    Side reactions that occur along with the conversion of alkali cellulose to cellulose xanthate are responsible for the orange color of the xanthate crumb and also the resulting viscose solution. The orange cellulose xanthate crumb is dissolved in dilute sodium hydroxide at 15 to 20 °C under high-shear mixing conditions to obtain a viscous orange colored solution called "viscose", which is the basis for the manufacturing process. The viscose solution is then filtered (to get out the insoluble fiber material) and is deaerated.

    Dissolving

    The yellow crumb is dissolved in aqueous caustic solution. The large xanthate substituents on the cellulose force the chains apart, reducing the interchain hydrogen bonds and allowing water molecules to solvate and separate the chains, leading to solution of the otherwise insoluble cellulose. Because of the blocks of un-xanthated cellulose in the crystalline regions, the yellow crumb is not completely soluble at this stage. Because the cellulose xanthate solution (or more accurately, suspension) has a very high viscosity, it has been termed "viscose".

    Ripening

    The viscose is allowed to stand for a period of time to "ripen". Two important process occur during ripening: Redistribution and loss of xanthate groups. The reversible xanthation reaction allows some of the xanthate groups to revert to cellulosic hydroxyls and free CS2. This free CS2 can then escape or react with other hydroxyl on other portions of the cellulose chain. In this way, the ordered, or crystalline, regions are gradually broken down and more complete solution is achieved. The CS2 that is lost reduces the solubility of the cellulose and facilitates regeneration of the cellulose after it is formed into a filament. (C6H9O4O-SC-SNa)n + nH2O ---> (C6H10O5)n + nCS2 + nNaOH 
     

    Filtering

    The viscose is filtered to remove undissolved materials that might disrupt the spinning process or cause defects in the rayon filament.

    Degassing

    Bubbles of air entrapped in the viscose must be removed prior to extrusion or they would cause voids, or weak spots, in the fine rayon filaments

    Spinning - (Wet Spinning)

    Production of Viscose Rayon Filament: The viscose solution is metered through a spinnerette into a spin bath containing sulphuric acid (necessary to acidify the sodium cellulose xanthate), sodium sulphate (necessary to impart a high salt content to the bath which is useful in rapid coagulation of viscose), and zinc sulphate (exchange with sodium xanthate to form zinc xanthate, to cross link the cellulose molecules).
    Once the cellulose xanthate is neutralized and acidified, rapid coagulation of the rayon filaments occurs which is followed by simultaneous stretching and decomposition of cellulose xanthate to regenerated cellulose. Stretching and decomposition are vital for getting the desired tenacity and other properties of rayon. Slow regeneration of cellulose and stretching of rayon will lead to greater areas of crystallinity within the fiber, as is done with high-tenacity rayons.
    The dilute sulphuric acid decomposes the xanthate and regenerates cellulose by the process of wet spinning. The outer portion of the xanthate is decomposed in the acid bath, forming a cellulose skin on the fiber. Sodium and zinc sulphates control the rate of decomposition (of cellulose xanthate to cellulose) and fiber formation.
    (C6H9O4O-SC-SNa)n + (n/2)H2SO4 --> (C6H10O5)n + nCS2 + (n/2)Na2SO4
    Elongation-at-break is seen to decrease with an increase in the degree of crystallinity and orientation of rayon.

    Drawing

    The rayon filaments are stretched while the cellulose chains are still relatively mobile. This causes the chains to stretch out and orient along the fiber axis. As the chains become more parallel, interchain hydrogen bonds form, giving the filaments the properties necessary for use as textile fibers

    Washing

    The freshly regenerated rayon contains many salts and other water soluble impurities which need to be removed. Several different washing techniques may be used

    Cutting

    If the rayon is to be used as staple (i.e., discreet lengths of fiber), the group of filaments (termed "tow") is passed through a rotary cutter to provide a fiber which can be processed in much the same way as cotton.