Difference between revisions of "Polyamide"
m (Text replace - "\[http:\/\/cameo\.mfa\.org\/materials\/fullrecord\.asp\?name=([^\s]+)\s(.*)\]" to "$2") |
|||
| Line 1: | Line 1: | ||
== Description == | == Description == | ||
| − | Synthetic ([[nylon|nylon]]) and natural ([[protein|protein]]) polyamides are made by polymerizing | + | Synthetic ([[nylon|nylon]]) and natural ([[protein|protein]]) polyamides are made by polymerizing an acid group (COO-) from one molecule with an amine (NH2) on another molecule. Two common natural polyamides include wool and silk. The most famous synthetic polyamides are nylon 6,6, and nylon 6. Nylon 6,6 was developed a textile fiber, called fiber #66, in the early 1930s by a scientist working at DuPont, W. H. Carothers. The name “nylon 6,6” was adopted by DuPont in 1938 when the polymer went into mass production. Nylon 6 was developed in Germany by chemist Paul Schlack, who worked for I.G. Farben and though the chemistry is slightly different, the final material has similar properties to nylon 6,6. Nylons are thermoplastic resins that are characterized by their high degree of toughness, strength and durability along with their resistance to chemicals and heat. They are manufactured as bristles, fibers, molding powders, sutures, adhesives, and coatings. The most important examples of polyamides are the various kinds of nylon. See also [[Aramid fiber|aramid]]. |
== Synonyms and Related Terms == | == Synonyms and Related Terms == | ||
| Line 9: | Line 9: | ||
Examples: Nylon® [Du Pont]; Technyl® [Rhodia]; Ultramid® [BASF]; Amilan® [Toray]; Durethan® [Lanxess]; | Examples: Nylon® [Du Pont]; Technyl® [Rhodia]; Ultramid® [BASF]; Amilan® [Toray]; Durethan® [Lanxess]; | ||
| − | == | + | == Physical and hCemical Properties == |
| − | Soluble in formic acid, dimethylformamide, m-cresol. | + | * Should not be ingested<ref>https://www.bfr.bund.de/cm/349/polyamide-kitchen-utensils-keep-contact-with-hot-food-as-brief-as-possible.pdf</ref>. Safe for handling with bare hands. |
| − | + | * Soluble in formic acid, dimethylformamide, m-cresol. | |
| − | Insoluble in methanol, diethyl ether, hydrocarbons. | + | * Insoluble in methanol, diethyl ether, hydrocarbons. |
| − | + | * Burns with orange-yellow flame, blue smoke and smells like burnt horn. | |
| − | Burns with orange-yellow flame, blue smoke and smells like burnt horn. | ||
== Comparisons == | == Comparisons == | ||
| Line 26: | Line 25: | ||
| − | + | == Resources and Citations == | |
| − | == | + | <references/> |
* G.S.Brady, ''Materials Handbook'', McGraw-Hill Book Co., New York, 1971 | * G.S.Brady, ''Materials Handbook'', McGraw-Hill Book Co., New York, 1971 | ||
Revision as of 12:50, 26 July 2020
Description
Synthetic (Nylon) and natural (Protein) polyamides are made by polymerizing an acid group (COO-) from one molecule with an amine (NH2) on another molecule. Two common natural polyamides include wool and silk. The most famous synthetic polyamides are nylon 6,6, and nylon 6. Nylon 6,6 was developed a textile fiber, called fiber #66, in the early 1930s by a scientist working at DuPont, W. H. Carothers. The name “nylon 6,6” was adopted by DuPont in 1938 when the polymer went into mass production. Nylon 6 was developed in Germany by chemist Paul Schlack, who worked for I.G. Farben and though the chemistry is slightly different, the final material has similar properties to nylon 6,6. Nylons are thermoplastic resins that are characterized by their high degree of toughness, strength and durability along with their resistance to chemicals and heat. They are manufactured as bristles, fibers, molding powders, sutures, adhesives, and coatings. The most important examples of polyamides are the various kinds of nylon. See also aramid.
Synonyms and Related Terms
PA; nylon; protein; aramid; poliamida (Esp.); polyamide (Fr.); poliammide (It.); poliamida (Port.)
Examples: Nylon® [Du Pont]; Technyl® [Rhodia]; Ultramid® [BASF]; Amilan® [Toray]; Durethan® [Lanxess];
Physical and hCemical Properties
- Should not be ingested[1]. Safe for handling with bare hands.
- Soluble in formic acid, dimethylformamide, m-cresol.
- Insoluble in methanol, diethyl ether, hydrocarbons.
- Burns with orange-yellow flame, blue smoke and smells like burnt horn.
Comparisons
Properties of Synthetic Fibers
General Characteristics of Polymers
Physical Properties for Selected Thermoplastic Resins
Resources and Citations
- G.S.Brady, Materials Handbook, McGraw-Hill Book Co., New York, 1971
- Theodore J. Reinhart, 'Glossary of Terms', Engineered Plastics, ASM International, 1988
- Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
- Hoechst Celanese Corporation, Dictionary of Fiber & Textile Technology (older version called Man-made Fiber and Textile Dictionary, 1965), Hoechst Celanese Corporation, Charlotte NC, 1990
- Rosalie Rosso King, Textile Identification, Conservation, and Preservation, Noyes Publications, Park Ridge, NJ, 1985
- Pam Hatchfield, Pollutants in the Museum Environment, Archetype Press, London, 2002
- Thomas C. Jester (ed.), Twentieth-Century Building Materials, McGraw-Hill Companies, Washington DC, 1995
- Encyclopedia Britannica, http://www.britannica.com Comment: Nylon. Encyclopædia Britannica. Retrieved May 25, 2003, from Encyclopædia Britannica Premium Service.
- Art and Architecture Thesaurus Online, http://www.getty.edu/research/tools/vocabulary/aat/, J. Paul Getty Trust, Los Angeles, 2000
- Website address 1 Comment: www.nswpmith.com.au/historyofplastics.html