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Nylon 6 or polycaprolactam is a polymer developed by Paul Schlack at IG Farben to reproduce the properties of nylon 6,6 without violating the patent on its production. Unlike most other nylons, nylon 6 is not a condensation polymer, but instead is formed by ring-opening polymerization. This makes it a special case in the comparison between condensation and addition polymers. Its competition with nylon 6,6 and the example it set have also shaped the economics of the synthetic fiber industry. It was given the trademark Perlon in the year 1952.

Contents 1 Synthesis 2 Properties 3 Applications 4 External links

Nylon 6 begins as pure caprolactam. As caprolactam has 6 carbon atoms, it got the name Nylon-6.

When caprolactam is heated at about 533 K in an inert atmosphere of nitrogen for about 4-5 hours, the ring breaks and undergoes polymerization. Then the molten mass is passed through spinnerets to form fibres of Nylon 6.

During polymerization, the peptide bond within each caprolactam molecule is broken, with the active groups on each side re-forming two new bonds as the monomer becomes part of the polymer backbone.

Unlike nylon 6,6, in which the direction of the amide bond reverses at each bond, all nylon 6 amide bonds lie in the same direction (see figure). Nylon 6 therefore resembles natural polypeptides more closely; in fact, caprolactam would become an amino acid if it were hydrolyzed. This difference has little effect on the polymer's mechanical or chemical properties, but is sufficient to create a legal distinction.

1. Nylon 6 fibres are tough, possessing high tensile strength.
2. Fibres have high elasticity and lustre.
3. Highly resistant to abrasion, chemicals like acids, alkalis, etc.
4. They are wrinkle proof.

1. Bristles for toothbrushes, sutures for surgery, etc.
2. Manufacture of hosiery, knitted garments, etc.
3. Manufacture of a large variety of threads, ropes, filaments, nets, tire cords, etc.

• Links to external chemical sources