Aramid fibers, short for aromatic polyamide, are a class of heat-resistant and strong synthetic fibers. They are used in aerospace and military applications, for ballistic-rated body armorfabric and ballistic composites, in marine cordage, marine hull reinforcement, as an asbestos substitute,[1] and in various lightweight consumer items ranging from phone cases to tennis rackets.
The chain molecules in the fibers are highly oriented along the fiber axis. As a result, a higher proportion of the chemical bond contributes more to fiber strength than in many other synthetic fibers. Aramids have a very high melting point (>500 °C (932 °F)).
Structure of Twaron and Kevlar. The aromatic rings appear as hexagons. The rings are attached alternately to either two NH groups or two CO groups. The attachment points on each ring are diametrically opposite each other, meaning this is classed as a para-aramid.
Aromatic in the longer name refers to the presence of aromatic rings of six carbon atoms. In aramids these rings are connected via amide linkages each comprising a CO group attached to an NH group.
In order to meet the FTC definition of an aramid,[4] at least 85% of these linkages must be attached to two aromatic rings.[5] Below 85%, the material is instead classed as nylon.[4]
Para-aramids and meta-aramids
Aramids are divided into two main types according to where the linkages attach to the rings. Numbering the carbon atoms sequentially around a ring, para-aramids have the linkages attached at positions 1 and 4, while meta-aramids have them at positions 1 and 3.[6] That is, the attachment points are diametrically opposite each other in para-aramids, and two atoms apart in meta-aramids. The illustration thus shows a para-aramid.
History
Aromatic polyamides were first introduced in commercial applications in the early 1960s, with a meta-aramid fiber produced by DuPont as HT-1 and then under the trade name Nomex.[7] This fiber, which handles similarly to normal textile apparel fibers, is characterized by its excellent resistance to heat, as it neither melts nor ignites in normal levels of oxygen. It is used extensively in the production of protective apparel, air filtration, thermal and electrical insulation, as well as a substitute for asbestos.
Meta-aramids are also produced in the Netherlands and Japan by Teijin Aramid under the trade name Teijinconex,[7] and by Toray under the trade name Arawin, in China by Yantai Tayho under the trade name New Star and by SRO Group under the trade name X-Fiper, and a variant of meta-aramid in France by Kermel under the trade name Kermel.
Based on earlier research by Monsanto Company and Bayer, para-aramid fiber with much higher tenacity and elastic modulus was also developed in the 1960s and 1970s by DuPont and AkzoNobel, both profiting from their knowledge of rayon, polyester and nylon processing. In 1973, DuPont was the first company to introduce a para-aramid fiber, calling it Kevlar; this remains one of the best-known[citation needed] para-aramids and/or aramids.
In 1978, Akzo introduced a similar fiber with roughly the same chemical structure calling it Twaron. Due to earlier patents on the production process, Akzo and DuPont engaged in a patent dispute in the 1980s. Twaron subsequently came under the ownership of the Teijin Aramid Company. In 2011, Yantai Tayho introduced similar fiber which is called Taparan in China (see Production).
Para-aramids are used in many high-tech applications, such as aerospace and military applications, for "bullet-proof" body armorfabric.
Both meta-aramid and para-aramid fiber can be used to make aramid paper. Aramid paper is used as electrical insulation materials and construction materials to make honeycomb core. Dupont made aramid paper during the 1960s, calling it Nomex paper. Yantai Metastar Special Paper introduced an aramid paper in 2007, which is called metastar paper. Both Dupont and Yantai Metastar make meta-aramid and para-aramid paper.[citation needed]
Health
During the 1990s, an in vitro test of aramid fibers showed they exhibited "many of the same effects on epithelial cells as did asbestos, including increased radiolabelednucleotide incorporation into DNA and induction of ODC (ornithine decarboxylase) enzyme activity", raising the possibility of carcinogenic implications.[8] However, in 2009, it was shown that inhaled aramid fibrils are shortened and quickly cleared from the body and pose little risk.[9] A declaration of interest correction was later provided by the author of the study stating that "This review was commissioned and funded by DuPont and Teijin Aramid, but the author alone was responsible for the content and writing of the paper."[10]
Production
World capacity of para-aramid production was estimated at about 41,000 t (40,000 long tons; 45,000 short tons) per year in 2002 and increases each year by 5–10%.[11] In 2007 this means a total production capacity of around 55,000 tonnes per year.[citation needed]
Polymer preparation
Aramids are generally prepared by the reaction between an amine group and a carboxylic acidhalide group. Simple AB homopolymers have the connectivity −(NH−C6H4−CO)n−.
Well-known aramid polymers such as Kevlar, Twaron, Nomex, New Star, and Teijinconex) are prepared from diamine and diacid (or equivalent) precursors. These polymers can be further classified according to the linkages on the aromatic subunits. Nomex, Teijinconex, and New Star contain predominantly the meta-linkage. They are called poly-metaphenylene isophthalamides (MPIAs). By contrast, Kevlar and Twaron both feature para-linkages. They are called p-phenylene terephthalamides (PPTAs). PPTA is a product of p-phenylene diamine (PPD) and terephthaloyl dichloride (TDC or TCl).
Production of PPTA relies on a co-solvent with an ionic component (calcium chloride, CaCl2) to occupy the hydrogen bonds of the amide groups, and an organic component (N-methyl pyrrolidone, NMP) to dissolve the aromaticpolymer. This process was invented by Leo Vollbracht at Akzo. Apart from the carcinogenicHMPT, still no practical alternative of dissolving the polymer is known. The use of the NMP/CaCl2 system led to an extended patent dispute between Akzo and DuPont.
Spinning
After production of the polymer, the aramid fiber is produced by spinning the dissolved polymer to a solid fiber from a liquid chemical blend. Polymer solvent for spinning PPTA is generally 100% anhydroussulfuric acid (H2SO4).
Besides meta-aramids like Nomex, other variations belong to the aramid fiber range. These are mainly of the copolyamide type, best known under the brand name Technora, as developed by Teijin and introduced in 1976. The manufacturing process of Technora reacts PPD and 3,4'-diaminodiphenylether (3,4'-ODA) with terephthaloyl chloride (TCl).[12]
This relatively simple process uses only one amide solvent, and therefore spinning can be done directly after the polymer production.
Aramid fiber characteristics
Aramids share a high degree of orientation with other fibers such as ultra-high-molecular-weight polyethylene, a characteristic that dominates their properties.
^The full definition of aramid fibre is "a manufactured fiber in which the fiber-forming substance is a long-chain synthetic polyamide in which at least 85% of the amide linkages, ( ) are attached directly to two aromatic rings", with a diagram between the parentheses which shows a vertically oriented CO group attached horizontally to an NH group. There is an incoming bond to the C atom and an outgoing one from the NH group.
^Position 1 is simply chosen as the point where one of the chains is attached. We then count around the ring in the shortest direction until we reach the other one.
^Marsh, J. P.; Mossman, B. T.; Driscoll, K. E.; Schins, R. F.; Borm, P. J. A. (1 January 1994). "Effects of Aramid, a high Strength Synthetic Fiber, on Respiratory Cells in Vitro". Drug and Chemical Toxicology. 17 (2): 75–92. doi:10.3109/01480549409014303. PMID8062644.
