Nylon

Nylon 6,6
Density	1.15 g/cm3
Electrical conductivity (σ)	10−12 S/m
Thermal conductivity	0.25 W/(m·K)
Melting point	463–624 K 190–350 °C 374–663 °F

Nylon is a generic designation for a family of synthetic polymers, based on aliphatic or semi-aromatic polyamides. Nylon is a thermoplastic silky material^[1] that can be melt-processed into fibers, films or shapes.^[2]:2

Nylon was the first commercially successful synthetic thermoplastic polymer.^[3] DuPont began its research project in 1930. The first example of nylon (nylon 6,6) was produced using diamines on February 28, 1935, by Wallace Carothers at DuPont's research facility at the DuPont Experimental Station.^[4][5] In response to Carothers' work, Paul Schlack at IG Farben developed nylon 6, a different formulation based on caprolactam, on January 29, 1938.^[6]:10[7]

Nylon was first used commercially in a nylon-bristled toothbrush in 1938,^[8][9] followed more famously in women's stockings or "nylons" which were shown at the 1939 New York World's Fair and first sold commercially in 1940.^[10] During World War II, almost all nylon production was diverted to the military for use in parachutes and parachute cord. Wartime uses of nylon and other plastics greatly increased the market for the new materials.^[11]

Nylon is made of repeating units linked by peptide bonds.^[3][12] Commercially, nylon polymer is made by reacting monomers which are either lactams, acid/amines or stoichiometric mixtures of diamines (-NH₂) and diacids (-COOH). Mixtures of these can be polymerized together to make copolymers. Nylon polymers can be mixed with a wide variety of additives to achieve many different property variations. Nylon polymers have found significant commercial applications in fabric and fibers (apparel, flooring and rubber reinforcement), in shapes (molded parts for cars, electrical equipment, etc.), and in films (mostly for food packaging).^[13]

History

DuPont and the invention of Nylon

DuPont, founded by Éleuthère Irénée du Pont, first produced gunpowder and later cellulose-based paints. Following WWI, DuPont produced synthetic ammonia and other chemicals. DuPont began experimenting with the development of cellulose based fibres, eventually producing the synthetic fibre rayon. DuPont's experience with rayon was an important precursor to its development and marketing of nylon.^{[14]:8,64,236}

DuPont's invention of nylon spanned a nine-year period, ranging from the start of the project in 1930 to its exhibition at the World Fair in New York in 1939.^[14] The project grew from a new structure at DuPont, suggested by Charles Stine in 1927, in which the chemical department would be composed of several small research teams that would focus on “pioneering research” in chemistry and would “lead to practical applications”.^[14]:92 Harvard instructor Wallace Hume Carothers was hired to direct the polymer research group. Initially he was allowed to focus on pure research, building on and testing the theories of German chemist Hermann Staudinger.^[15] He was very successful as researches he undertook greatly improved the knowledge of polymers and contributed to science.^[16]

In the spring of 1930, Carothers and his team had already synthesized two new polymers. One was neoprene, a synthetic rubber greatly used during the war. The other was a white elastic but strong paste that would later become nylon. After these discoveries Carother’s team was made to shift its research from a more pure research approach investigating general polymerization to a more practically-focused goal of finding “one chemical combination that would lend itself to industrial applications”.^[14]:94

It wasn’t until the beginning of 1935 that a polymer called "polymer 6-6" was finally produced. The first example of nylon (nylon 6,6) was produced by Wallace Caruthers on February 28, 1935, at DuPont's research facility at the DuPont Experimental Station.^[4] It had all the desired properties of elasticity and strength. However, it also required a complex manufacturing process that would become the basis of industrial production in the future. DuPont obtained a patent for the polymer in September 1938,^[17] and quickly achieved a monopoly of the fibre.^[16]

The production of nylon required interdepartmental collaboration between three departments at DuPont: the Department of Chemical Research, the Ammonia Department, and the Department of Rayon. Some of the key ingredients of nylon had to be produced using high pressure chemistry, the main area of expertise of the Ammonia Department. Nylon was considered a “godsend to the Ammonia Department”,^[14] which had been in financial difficulties. The reactants of nylon soon constituted half of the Ammonia department’s sales and helped them come out of the period of the Great Depression by creating jobs and revenue at DuPont.^[14]

DuPont's nylon project demonstrated the importance of chemical engineering in industry, helped create jobs, and furthered the advancement of chemical engineering techniques. In fact, it developed a chemical plant that provided 1800 jobs and used the latest technologies of the time, which are still used as a model for chemical plants today.^[14] “The success of the nylon project thus had to do with its ability to achieve the rapid mobilization of a large number of DuPont’s chemists and engineers”.^{[14]:100–101} The first nylon plant was located at Seaford, Delaware, beginning commercial production on December 15, 1939. On October 26, 1995, the Seaford plant was designated a National Historic Chemical Landmark by the American Chemical Society.^[18]

Origin of the name

DuPont went through an extensive process to generate names for its new product.^{[16]:138–139} In 1940, John W. Eckelberry of DuPont stated that the letters "nyl" were arbitrary and the "on" was copied from the suffixes of other fibers such as cotton and Rayon. A later publication by DuPont (Context, vol. 7, no. 2, 1978) explained that the name was originally intended to be "No-Run" ("run" meaning "unravel"), but was modified to avoid making such an unjustified claim. Since the products were not really run-proof, the vowels were swapped to produce "nuron", which was changed to "nilon" "to make it sound less like a nerve tonic". For clarity in pronunciation, the "i" was changed to "y".^[10][19]

Early marketing strategies

An important part of nylon’s popularity stems from DuPont’s marketing strategy. The fibre was promoted to increase demand before the product was available to the general market. Nylon’s commercial announcement occurred on October 27, 1938, at the final session of the Herald Tribune's yearly "Forum on Current Problems", on the site of the approaching New York City world's fair.^[15][16]:141 The “first man-made organic textile fiber” which was derived from “coal, water and air” and promised to be “as strong as steel, as fine as the spider’s web” was received enthusiastically by the audience, many of them middle-class women, and made the headlines of most newspapers.^[16]:141 Nylon was introduced as part of "The world of tomorrow" at the 1939 New York World's Fair^[20] and was featured at DuPont's "Wonder World of Chemistry" at the Golden Gate International Exposition in San Francisco in 1939.^[15][21] Actual nylon stockings were not shipped to selected stores in the national market until May 15, 1940. However, a limited number were released for sale in Delaware before that.^{[16]:145–146} The first public sale of nylon stockings occurred on October 24, 1939, in Wilmington, Delaware. 4,000 pairs of stockings were available, all of which were sold within three hours.^[15]

Another added bonus to the campaign was that it meant reducing silk imports from Japan, an argument that won over many wary customers. Nylon was even mentioned by President Roosevelt’s cabinet, which addressed its “vast and interesting economic possibilities” five days after the material was formally announced.^[16]

However, the early excitement over nylon also caused problems. It fueled unreasonable expectations that nylon would be better than silk, a miracle fabric as strong as steel that would last forever and never run.^{[16]:145–147[10]} Realizing the danger of claims such as “New Hosiery Held Strong as Steel” and “No More Runs”, Du Pont scaled back the terms of the original announcement, especially those stating that nylon would possess the strength of steel.^[16]

Also, DuPont executives marketing nylon as a revolutionary man-made material did not at first realize that some consumers experienced a sense of unease and distrust, even fear, towards synthetic fabrics.^{[16]:126–128} A particularly damaging news story, drawing on DuPont's 1938 patent for the new polymer, suggested that one method of producing nylon might be to use cadaverine, a chemical extracted from corpses. Although scientists asserted that cadaverine was also extracted by heating coal, the public often refused to listen, as in the case of a woman who confronted one of the lead scientists at DuPont and refused to accept that the rumour was not true.^{[16]:146–147}

DuPont changed its campaign strategy, emphasizing that nylon was made from “coal, air and water”, and started focusing on the personal and aesthetic aspects of nylon, rather than its intrinsic qualities.^{[16]:146–147} Nylon was thus domesticated,^[16]:151-152 and attention shifted to the material and consumer aspect of the fiber with slogans like “If it’s nylon, it’s prettier, and oh! How fast it dries!”.^[14]:2

Production of nylon fabric

After nylon’s nationwide release in 1940, production was increased. 1300 tons of the fabric were produced during 1940.^[14]:100 During their first year on the market, 64 million pairs of nylon stockings were sold.^[14]:101

While nylon was marketed as the durable and indestructible material of the people, it was sold at almost twice the price of silk stockings ($4.27 per pound of nylon versus $2.79 per pound of silk).^[14]:101 Sales of nylon stockings were strong in part due to changes in women’s fashion. As Lauren Olds explains: “by 1939 [hemlines] had inched back up to the knee, closing the decade just as it started off”. The shorter skirts were accompanied by a demand for stockings that offered fuller coverage without the use of garters to hold them up.^[22] H

However, as of February 11, 1942, nylon production was redirected from being a consumer material to one used by the military.^[15] DuPont's production of nylon stockings and other lingerie stopped, and most manufactured nylon was used to make parachutes and tents for World War II.^[23]

Once the war ended, the return of nylon was awaited with great anticipation. Although DuPont projected yearly production of 360 million pairs of stockings, there were delays in converting back to consumer rather than wartime production.^[15] In 1946, the demand for nylon stockings could not be satisfied, which led to the Nylon Riots. In one case, an estimated 40,000 people lined up in Pittsburgh to buy 13,000 pairs of nylons.^[10] In the meantime, women cut up nylon tents and parachutes left from the war in order to make blouses and wedding dresses.^[24][25] Between the end of the war and 1952, production of stockings and lingerie used 80% of the world’s nylon. DuPont put a lot of focus on catering to the civilian demand, and continually expanded its production.

Introduction of nylon blends

As pure nylon hosiery was sold in a wider market, problems became apparent. Nylon stockings were found to be fragile, in the sense that the thread often tended to unravel lengthwise, creating ‘runs’.^[14]:101 People also reported that pure nylon textiles could be uncomfortable due to nylon's lack of absorbency.^[26] Moisture stayed inside the fabric near the skin under hot or moist conditions instead being "wicked" away.^[27] Nylon fabric could also be itchy, and tended to cling and sometimes spark as a result of static electrical charge built up by friction.^[28][29] Also, under some conditions stockings could decompose^[16] turning back into nylon's original components of air, coal, and water. Scientists explained this as a result of air pollution, attributing it to London smog in 1952, as well as poor air quality in New York and Los Angeles.^[30][31][32]

The solution found to problems with pure nylon fabric was to blend nylon with other existing fibres or polymers such as cotton, polyester, and spandex. This led to the development of a wide array of blended fabrics. The new nylon blends retained the desirable properties of nylon (elasticity, durability, ability to be dyed) and kept clothes prices low and affordable.^[23]:2 As of 1950, the New York Quartermaster Procurement Agency (NYQMPA), which developed and tested textiles for the army and navy, had committed to developing a wool-nylon blend. They were not the only ones to introduce blends of both natural and synthetic fibres. America's Textile Reporter referred to 1951 as the "Year of the blending of the fibers".^[33] Fabric blends included mixes like "Bunara" (wool-rabbit-nylon) and "Casmet" (wool-nylon-fur).^[34] In Britain in November 1951, the inaugural address of the 198th session of the Royal Society for the Encouragement of Arts, Manufactures and Commerce focused on the blending of textiles.^[35]

DuPont's Fabric Development Department cleverly targeted French fashion designers, supplying them with fabric samples. In 1955, designers such as Coco Chanel, Jean Patou, and Christian Dior showed gowns created with DuPont fibers, and fashion photographer Horst P. Horst was hired to document their use of DuPont fabrics.^[10] American Fabrics credited blends with providing "creative possibilities and new ideas for fashions which had been hitherto undreamed of."^[34]

Longer-term popularity

In spite of oil shortages in the 1970s, consumption of nylon textiles continued to grow by 7.5 per cent per annum between the 1960s and 1980s.^[36] Overall production of synthetic fibres, however, dropped from 63% of the worlds textile production in 1965, to 45% of the world's textile production in early 1970s.^[36] The appeal of "new" technologies wore off, and nylon fabric “was going out of style in the 1970s”.^[14] Also, consumers became concerned about environmental costs throughout the production cycle: obtaining the raw materials (oil), energy use during production, waste produced during creation of the fibre, and eventual waste disposal of materials that were not biodegradable.^[36] Synthetic fibres have not dominated the market since the 1950s and 1960s. As of 2008, nylon continued to represent about 12% (8 million pounds) of the world’s production of synthetic fibres.^[10]

Although pure nylon has many flaws and is now rarely used, its derivatives have greatly influenced and contributed to society. From scientific discoveries relating to the production of plastics and polymerization, to economic impact during the depression and the changing of women’s fashion, nylon was a revolutionary product.^[10] The first flag planted on the moon, in a symbolic gesture of celebration, was made of nylon. The flag itself cost $5.50, but had to have a specially-designed flagpole with a horizontal bar so that it would appear to "fly".^[37][38] “Nylon is one of the great symbols of the American century, on a par no doubt with Coca-Cola in the consumer dreams of 20th century men and women. [...] it is not only a technologically advanced product, it has also captured the public’s imagination [...]: nylon as an object of desire”.^[14]:182

Chemistry

External video

“Making Nylon“, Bob Burk, CHEM 1000, Carleton University, Ottawa, Canada

“Making Nylon 6,6“

“Nylon production“, Royal Society of Chemistry

“Nylon and Rayon Manufacture 1949“, Encyclopedia Britannica Films

Nylons are condensation copolymers, formed by reacting difunctional monomers containing equal parts of amine and carboxylic acid, so that amides are formed at both ends of each monomer in a process analogous to polypeptide biopolymers. Most nylons are made from the reaction of a dicarboxylic acid with a diamine (e.g. PA66) or a lactam or amino acid with itself (e.g. PA6).^[39] In the first case, the "repeating unit" consists of one of each monomer, so that they alternate in the chain, similar to the so-called ABAB structure of polyesters and polyurethanes. Since each monomer in this copolymer has the same reactive group on both ends, the direction of the amide bond reverses between each monomer, unlike natural polyamide proteins, which have overall directionality: C terminal → N terminal. In the second case (so called AA), the repeating unit corresponds to the single monomer.^{[6]:45-50[40]}

Types of nylon

Nylon 66

Wallace Carothers at DuPont patented nylon 66 using amides.^[17][41][42] In the case of nylons that involve reaction of a diamine and a dicarboxylic acid, it is difficult to get the proportions exactly correct, and deviations can lead to chain termination at molecular weights less than a desirable 10,000 daltons (u). To overcome this problem, a crystalline, solid "nylon salt" can be formed at room temperature, using an exact 1:1 ratio of the acid and the base to neutralize each other. The salt is crystallized to purify it and obtain the desired precise stoichiometry. Heated to 285 °C (545 °F), the salt reacts to form nylon polymer with the production of water.

Nylon 6

Carothers overlooked the possibility of using lactams. That synthetic route was developed by Paul Schlack at IG Farben, leading to nylon 6, or polycaprolactam — formed by a ring-opening polymerization. The peptide bond within the caprolactam is broken with the exposed active groups on each side being incorporated into two new bonds as the monomer becomes part of the polymer backbone.

The 428 °F (220 °C) melting point of nylon 6 is lower than the 509 °F (265 °C) melting point of nylon 66.^[43]

Nylon 510

Nylon 510, made from pentamethylene diamine and sebacic acid, was studied by Carothers even before nylon 66 and has superior properties, but is more expensive to make. In keeping with this naming convention, "nylon 6,12" or "PA 612" is a copolymer of a 6C diamine and a 12C diacid. Similarly for PA 510 PA 611; PA 1012, etc. Other nylons include copolymerized dicarboxylic acid/diamine products that are not based upon the monomers listed above. For example, some fully aromatic nylons (known as "aramids") are polymerized with the addition of diacids like terephthalic acid (→ Kevlar, Twaron) or isophthalic acid (→ Nomex), more commonly associated with polyesters. There are copolymers of PA 66/6; copolymers of PA 66/6/12; and others. In general linear polymers are the most useful, but it is possible to introduce branches in nylon by the condensation of dicarboxylic acids with polyamines having three or more amino groups.

The general reaction is:

Two molecules of water are given off and the nylon is formed. Its properties are determined by the R and R' groups in the monomers. In nylon 6,6, R = 4C and R' = 6C alkanes, but one also has to include the two carboxyl carbons in the diacid to get the number it donates to the chain. In Kevlar, both R and R' are benzene rings.

Industrial synthesis is usually done by heating the acids, amines or lactams to remove water, but in the laboratory, diacid chlorides can be reacted with diamines. For example, a popular demonstration of interfacial polymerization (the "nylon rope trick") is the synthesis of nylon 66 from adipoyl chloride and hexamethylene diamine.

Nylon 1,6

Nylons can also be synthesized from dinitriles using acid catalysis. For example, this method is applicable for preparation of nylon 1,6 from adiponitrile, formaldehyde and water.^[44] Additionally, nylons can be synthesized from diols and dinitriles using this method as well.^[45]

Nomenclature

The nomenclature used for nylon polymers was devised during the synthesis of the first simple aliphatic nylons and uses numbers to describe the number of carbons between acid and amine functions (including the carbon of the carboxylic acid). Subsequent use of cyclic and aromatic monomers required the use of letters or sets of letters. One number after "PA" for a homopolymer based on one monomer, and two numbers or sets of letters where there are two monomers. For copolymers the comonomers or pairs of comonomers are separated by slashes, as shown in the examples below.

• homopolymers :
  • PA 6 : [NH−(CH₂)₅−CO]_n made from ε-Caprolactam ;
  • PA 66 : [NH−(CH₂)₆−NH−CO−(CH₂)₄−CO]_n made from hexamethylenediamine and adipic acid;
• copolymers :
  • PA 6/66 : [NH-(CH₂)₆−NH−CO−(CH₂)₄−CO]_n−[NH−(CH₂)₅−CO]_m made from caprolactam, hexamethylenediamine and adipic acid ;
  • PA 66/610 : [NH−(CH₂)₆−NH−CO−(CH₂)₄−CO]_n−[NH−(CH₂)₆−NH−CO−(CH₂)₈−CO]_m made from hexamethylenediamine, adipic acid and sebacic acid.

In common usage, the prefix 'PA' or the name 'Nylon' are used interchangeably and are equivalent in meaning.

The term polyphthalamide (abbreviated to PPA) is used when 60% or more moles of the carboxylic acid portion of the repeating unit in the polymer chain is composed of a combination of terephthalic (TPA) and isophthalic (IPA) acids

Monomers

Nylon monomers are manufactured by a variety of routes, starting in most cases from crude oil but sometimes from biomass. Those in current production are described below.

Amino acids and lactams

• ε-Caprolactam: Crude oil → benzene → cyclohexane → cyclohexanone → cyclohexanone oxime → caprolactam
• 11-aminoundecanoic acid: Castor oil → ricinoleic acid → methylricinoleate → methyl-11-undecenoate → undecenoic acid → 11-undecenoic acid → 11-bromoundecanoic acid → 11-aminoundecanoic acid^[46]
• Laurolactam: Butadiene → cyclododecatriene → cyclododecane → cyclododecanone → cyclododecanone oxime → laurolactam

Diacids

• Adipic acid: Crude oil → benzene → cyclohexane → cyclohexanone + cyclohexanol → adipic acid
• Sebacic acid (decanedioic acid): Castor oil → ricinoleic acid → sebacic acid
• Terephthalic acid: Crude oil → p-xylene → terephthalic acid
• Isophthalic acid: Crude oil → m-xylene → isophthalic acid

Diamines

• Tetramethylene diamine (putrescine) Crude oil → propylene → acrylonitrile → succinonitrile → tetramethylene diamine
• Hexamethylene diamine (HMD): Crude oil → butadiene → adiponitrile → hexamethylene diamine
• 1,9-diaminononane: Crude oil → butadiene → 7-octen-1-al → 1,9-nonanedial → 1,9-diaminononane^[47]

2-methyl pentamethylene diamine is a by product of HMD production

• Trimethyl Hexamethylene diamine (TMD): Crude oil → propylene → acetone → isophorone → TMD
• m-xylylene diamine (MXD): Crude oil → m-xylene → isophthalic acid → isophthalonitrile → m-xylylene diamine^[48]

With increasing interest in biobased materials other monomers are being investigated: 1,5-pentanediamine (cadaverine) (PMD): starch (e.g. cassava) → glucose → lysine → PMD.^[49]

Polymers

Due to the large number of diamines, diacids and aminoacids that can be synthesized, many nylon polymers have been made experimentally and characterized to varying degrees. A smaller number have been scaled up and offered commercially, and these are detailed below.

Homopolymers

Homopolymer nylons derived from one monomer

Monomer	Polymer
caprolactam	6
11-aminoundecanoic acid	11
ω-aminolauric acid	12

Examples of these polymers that are or were commercially available

• PA6 Lanxess Durethan B^[50]
• PA11 Arkema Rilsan^[51]
• PA12 Evonik Vestamid L^[52]

Homopolymer polyamides derived from pairs of diamines and diacids (or diacid derivatives). Shown in the table below are polymers which are or have been offered commercially either as homopolymers or as a part of a copolymer.

	Putrescine	MPMD	HMD	MXD	Nonanediamine	Decanediamine	Dodecanediamine	bis(para-aminocyclohexyl)methane	trimethylhexamethylenediamine
Adipic acid	46	D6	66	MXD6
Sebacic acid	410		610			1010
Dodecanedioic acid			612				1212	PACM12
Terephthalic acid	4T	DT	6T		9T	10T	12T		TMDT
Isophthalic acid		DI	6I

Examples of these polymers that are or were commercially available

• PA46 DSM Stanyl^[53]
• PA410 DSM Ecopaxx^[54]
• PA4T DSM Four Tii^[55]
• PA66 DuPont Zytel^[56]

Copolymers

It is easy to make mixtures of the monomers or sets of monomers used to make nylons to obtain copolymers. This lowers crystallinity and can therefore lower the melting point.

Some copolymers that have been or are commercially available are listed below:

• PA6/66 DuPont Zytel^[57]
• PA6/6T BASF Ultramid T (6/6T copolymer)^[58]
• PA6I/6T DuPont Selar PA^[59]
• PA66/6T DuPont Zytel HTN^[58]
• PA12/MACMI EMS Grilamid TR^[60]

Blends

Most nylon polymers are miscible with each other allowing a range of blends to be made. The two polymers can react with one another by transamidation to form random copolymers.^[61]

According to their crystallinity, polyamides can be:

• semi-crystalline:
  • high crystallinity: PA46 and PA66;
  • low crystallinity: PAMXD6 made from m-xylylenediamine and adipic acid;
• amorphous: PA6I made from hexamethylenediamine and isophthalic acid.

According to this classification, PA66, for example, is an aliphatic semi-crystalline homopolyamide.

Flammability

Nylon clothing tends to be less flammable than cotton and rayon, but nylon fibres may melt and stick to skin.^[62][63]

Bulk properties

Above their melting temperatures, T_m, thermoplastics like nylon are amorphous solids or viscous fluids in which the chains approximate random coils. Below T_m, amorphous regions alternate with regions which are lamellar crystals.^[64] The amorphous regions contribute elasticity and the crystalline regions contribute strength and rigidity. The planar amide (-CO-NH-) groups are very polar, so nylon forms multiple hydrogen bonds among adjacent strands. Because the nylon backbone is so regular and symmetrical, especially if all the amide bonds are in the trans configuration, nylons often have high crystallinity and make excellent fibers. The amount of crystallinity depends on the details of formation, as well as on the kind of nylon.

Nylon 66 can have multiple parallel strands aligned with their neighboring peptide bonds at coordinated separations of exactly 6 and 4 carbons for considerable lengths, so the carbonyl oxygens and amide hydrogens can line up to form interchain hydrogen bonds repeatedly, without interruption (see the figure opposite). Nylon 510 can have coordinated runs of 5 and 8 carbons. Thus parallel (but not antiparallel) strands can participate in extended, unbroken, multi-chain β-pleated sheets, a strong and tough supermolecular structure similar to that found in natural silk fibroin and the β-keratins in feathers. (Proteins have only an amino acid α-carbon separating sequential -CO-NH- groups.) Nylon 6 will form uninterrupted H-bonded sheets with mixed directionalities, but the β-sheet wrinkling is somewhat different. The three-dimensional disposition of each alkane hydrocarbon chain depends on rotations about the 109.47° tetrahedral bonds of singly bonded carbon atoms.

When extruded into fibers through pores in an industry spinneret, the individual polymer chains tend to align because of viscous flow. If subjected to cold drawing afterwards, the fibers align further, increasing their crystallinity, and the material acquires additional tensile strength. In practice, nylon fibers are most often drawn using heated rolls at high speeds.^[65]

Block nylon tends to be less crystalline, except near the surfaces due to shearing stresses during formation. Nylon is clear and colorless, or milky, but is easily dyed. Multistranded nylon cord and rope is slippery and tends to unravel. The ends can be melted and fused with a heat source such as a flame or electrode to prevent this.

Nylons are hygroscopic, and will absorb or desorb moisture as a function of the ambient humidity. Variations in moisture content have several effects on the polymer. Firstly, the dimensions will change, but more importantly moisture acts as a plasticizer, lowering the glass transition temperature (T_g), and consequently the elastic modulus at temperatures below the T_g^[66]

When dry, polyamide is a good electrical insulator. However, polyamide is hygroscopic. The absorption of water will change some of the material's properties such as its electrical resistance. Nylon is less absorbent than wool or cotton.

Characteristics

The characteristic features of nylon 6,6 include:

• Pleats and creases can be heat-set at higher temperatures
• More compact molecular structure
• Better weathering properties; better sunlight resistance
• Softer "Hand"
• High melting point (256 °C/492.8 °F)
• Superior colorfastness
• Excellent abrasion resistance

On the other hand, nylon 6 is easy to dye, more readily fades; it has a higher impact resistance, a more rapid moisture absorption, greater elasticity and elastic recovery.

• 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, animals, as well as molds, mildew, rot and many chemicals
• Used in carpets and nylon stockings
• Melts instead of burning
• Used in many military applications
• Good specific strength
• Transparent to infrared light (−12 dB)^[67]

Uses

Fibers

Bill Pittendreigh, DuPont, and other individuals and corporations worked diligently during the first few months of World War II to find a way to replace Asian silk and hemp with nylon in parachutes. It was also used to make tires, tents, ropes, ponchos, and other military supplies. It was even used in the production of a high-grade paper for U.S. currency. At the outset of the war, cotton accounted for more than 80% of all fibers used and manufactured, and wool fibers accounted for nearly all of the rest. By August 1945, manufactured fibers had taken a market share of 25%, at the expense of cotton. After the war, because of shortages of both silk and nylon, nylon parachute material was sometimes repurposed to make dresses.^[68]

Nylon 6 and 66 fibers are used in carpet manufacture.

Nylon is one kind of fiber used in tire cord.

Shapes

Nylon resins are widely used in the automobile industry especially in the engine compartment.^[69][2]:514

Molded nylon is used in hair combs and mechanical parts such as machine screws, gears and other low- to medium-stress components previously cast in metal.^[70] Engineering-grade nylon is processed by extrusion, casting, and injection molding. 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.^[71][72] For use in tools such as spudgers, nylon is available in glass-filled variants which increase structural and impact strength and rigidity, and molybdenum disulfide-filled variants which increase lubricity. Its various properties also make it very useful as a material in additive manufacturing; specifically as a filament in consumer and professional grade fused deposition modeling 3D printers.^[73] Nylon can be used as the matrix material in composite materials, with reinforcing fibers like glass or carbon fiber; such a composite has a higher density than pure nylon.^[74] Such thermoplastic composites (25% to 30% glass fiber) are frequently used in car components next to the engine, such as intake manifolds, where the good heat resistance of such materials makes them feasible competitors to metals.^[75]

Nylon was used to make the stock of the Remington Nylon 66 rifle.^[76] The frame of the modern Glock pistol is made of a nylon composite.^[77]

Food packaging

Nylon resins are used as a component of food packaging films where an oxygen barrier is needed.^[13] Some of the terpolymers based upon nylon are used every day in packaging. Nylon has been used for meat wrappings and sausage sheaths.^[78] The high temperature resistance of nylon makes it useful for oven bags.^[79]

Filaments

Nylon filaments are primarily used in brushes especially toothbrushes^[8] and string trimmers. They are also used as monofilaments in fishing line. Nylon 610 and 612 are the most used polymers for filaments.

Its various properties also make it very useful as a material in additive manufacturing; specifically as a filament in consumer and professional grade fused deposition modeling 3D printers.^[73]

Other forms

Extruded Profiles

Nylon resins can be extruded into rods, tubes and sheets.^[2]:209

Powder Coating

Nylon powders are used to powder coat metals. Nylon 11 and nylon 12 are the most widely used.^[2]:53

Instrument strings

In the mid-1940s, classical guitarist Andrés Segovia mentioned the shortage of good guitar strings in the United States, particularly his favorite Pirastro catgut strings, to a number of foreign diplomats at a party, including General Lindeman of the British Embassy. A month later, the General presented Segovia with some nylon strings which he had obtained via some members of the DuPont family. Segovia found that although the strings produced a clear sound, they had a faint metallic timbre which he hoped could be eliminated.^[80]

Nylon strings were first tried on stage by Olga Coelho in New York in January, 1944.^[81]

In 1946, Segovia and string maker Albert Augustine were introduced by their mutual friend Vladimir Bobri, editor of Guitar Review. On the basis of Segovia's interest and Augustine's past experiments, they decided to pursue the development of nylon strings. DuPont, skeptical of the idea, agreed to supply the nylon if Augustine would endeavor to develop and produce the actual strings. After three years of development, Augustine demonstrated a nylon first string whose quality impressed guitarists, including Segovia, in addition to DuPont.^[80]

Wound strings, however, were more problematic. Eventually, however, after experimenting with various types of metal and smoothing and polishing techniques, Augustine was also able to produce high quality nylon wound strings.^[80]

Hydrolysis and degradation

All nylons are susceptible to hydrolysis, especially by strong acids, a reaction essentially the reverse of the synthetic reaction shown above. The molecular weight of nylon products so attacked drops, and cracks form quickly at the affected zones. Lower members of the nylons (such as nylon 6) are affected more than higher members such as nylon 12. This means that nylon parts cannot be used in contact with sulfuric acid for example, such as the electrolyte used in lead–acid batteries.

When being molded, nylon must be dried to prevent hydrolysis in the molding machine barrel since water at high temperatures can also degrade the polymer.^[82] The reaction is of the type:

Environmental impact, incineration and recycling

Berners-Lee calculates the average greenhouse gas footprint of nylon in manufacturing carpets at 5.43 kg CO₂ equivalent per kg, when produced in Europe. This gives it almost the same carbon footprint as wool, but with greater durability and therefore a lower overall carbon footprint.^[83]

Data published by PlasticsEurope indicates for nylon 66 a greenhouse gas footprint of 6.4 kg CO₂ equivalent per kg, and an energy consumption of 138 kJ/kg.^[84] When considering the environmental impact of nylon, it is important to consider the use phase. In particular when cars are lightweighted, significant savings in fuel consumption and CO₂ emissions are reduced.

Various nylons break down in fire and form hazardous smoke, and toxic fumes or ash, typically containing hydrogen cyanide. Incinerating nylons to recover the high energy used to create them is usually expensive, so most nylons reach the garbage dumps, decaying very slowly.^[85] Nylon is a robust polymer and lends itself well to recycling. Much nylon resin is recycled directly in a closed loop at the injection molding machine, by grinding sprues and runners and mixing them with the virgin granules being consumed by the molding machine.^[86]

Current market and forecast

As one of the largest engineering polymer families, the global demand of nylon resins and compounds was valued at roughly US$20.5 billion in 2013. The market is expected to reach US$30 billion by 2020 by following an average annual growth of 5.5%.^[87]

See also

References

Further reading

• Textiles by Sara J. Kadolph, ISBN 0-13-118769-4
• Kohan, Melvin (1995). Nylon Plastics Handbook. Munich: Carl Hanser Verlag. ISBN 1569901899. 

External links

Wikimedia Commons has media related to Nylon.

• Making Nylon, Bob Burk, CHEM 1000, Carleton University, Ottawa, Canada ]
• Polyamide Nylon Plastic
• "How Nylon Yarn Is Made", January 1946, Popular Science