Nylon 6
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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.
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Synthesis
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.
Properties
- Nylon 6 fibres are tough, possessing high tensile strength.
- Fibres have high elasticity and lustre.
- Highly resistant to abrasion, chemicals like acids, alkalis, etc.
- They are wrinkle proof.
- It has the potential to be used as a technical nutrient
Applications
- Bristles for toothbrushes, sutures for surgery, etc.
- Manufacture of hosiery, knitted garments, etc.
- Manufacture of a large variety of threads, ropes, filaments, nets, tire cords, etc.
External links
- The Promise of Nylon 6: A Case Study in Intelligent Product Design by William McDonough & Michael Braungart (available online through William McDonough's website: www.mcdonough.com)
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

