3rd class/polymer dep. Lect. 8/ Kevlar fibers Kevlar From Wikipedia, the free encyclopedia Kevlar Identifiers CAS number Properties 24938-64-5 Molecular formula [-CO-C6H4-CO-NH-C6H4NH-]n Kevlar is the registered trademark for a para-aramid synthetic fiber, related to other aramids such as Nomex and Technora. Developed by Stephanie Kwolek at DuPont in 1965,[1][2][3] this high-strength material was first commercially used in the early 1970s as a replacement for steel in racing tires. Typically it is spun into ropes or fabric sheets that can be used as such or as an ingredient in composite material components. Currently, Kevlar has many applications, ranging from bicycle tires and racing sails to body armor because of its high tensile strength-to-weight ratio; by this measure it is 5 times stronger than steel.[2] It is also used to make modern drumheads that withstand high impact. When used as a woven material, it is suitable for mooring lines and other underwater applications. A similar fiber called Twaron with roughly the same chemical structure was developed by Akzo in the 1970s; commercial production started in 1986, and Twaron is now manufactured by Teijin.[4][5] Production Kevlar does not dissolve easily. And it does not melt. (it decompose at 500 oC , while spinning the fibers required the product to be in a liquid state. 1 Lect. 8/ Kevlar fibers 3rd class/polymer dep. Then this problem is solved by Stephaine Kwolek and Herbert Blades by addition of lithium chloride or calcium chloride to the reactant solution as a catalyst. Kevlar is synthesized in solution from the monomers 1,4-phenylenediamine (para-phenylenediamine) and terephthaloyl chloride in a condensation reaction yielding hydrochloric acid as a byproduct. The result has liquid-crystalline behavior, and mechanical drawing orients the polymer chains in the fiber's direction. Hexamethylphosphoramide (HMPA) was the solvent initially used for the polymerization, but for safety reasons, DuPont replaced it by a solution of N-methyl-pyrrolidone and calcium chloride. As this process had been patented by Akzo (see above) in the production of Twaron, a patent war ensued.[9] The reaction of 1,4-phenylene-diamine (para-phenylenediamine) with terephthaloyl chloride yielding kevlar Kevlar (poly paraphenylene terephthalamide) production is expensive because of the difficulties arising from using concentrated sulfuric acid, needed to keep the water-insoluble polymer in solution during its synthesis and spinning. Several grades of Kevlar are available: 1. Kevlar K-29 – in industrial applications, such as cables, asbestos replacement, brake linings, and body/vehicle armor. 2. Kevlar K49 – high modulus used in cable and rope products. 3. Kevlar K100 – colored version of Kevlar 4. Kevlar K119 – higher-elongation, flexible and more fatigue resistant 5. Kevlar K129 – higher tenacity for ballistic applications 6. Kevlar AP – 15% higher tensile strength than K-29[10] 2 Lect. 8/ Kevlar fibers 3rd class/polymer dep. 7. Kevlar XP – lighter weight resin and KM2 plus fiber combination[11] 8. Kevlar KM2 – enhanced ballistic resistance for armor applications[12] The ultraviolet component of sunlight degrades and decomposes Kevlar, a problem known as UV degradation, and so it is rarely used outdoors without protection against sunlight.[citation needed] Structure and properties Molecular structure of Kevlar: bold represents a monomer unit, dashed lines indicate hydrogen bonds. When Kevlar is spun, the resulting fiber has a tensile strength of about 3,620 MPa,[13] and a relative density of 1.44. The polymer owes its high strength to the many inter-chain bonds. These inter-molecular hydrogen bonds form between the carbonyl groups and NH centers. Additional strength is derived from aromatic stacking interactions between adjacent strands. These interactions have a greater influence on Kevlar than the van der Waals interactions and chain length that typically influence the properties of other synthetic polymers and fibers such as Dyneema. The presence of salts and certain other impurities, especially calcium, could interfere with the strand interactions and care is taken to avoid inclusion in its production. Kevlar's structure consists of relatively rigid molecules which tend to form mostly planar sheet-like structures rather like silk protein.[14] Thermal properties Kevlar maintains its strength and resilience down to cryogenic temperatures (−196 °C); in fact, it is slightly stronger at low temperatures. At higher temperatures the tensile strength is immediately reduced by about 10–20%, and after some hours the strength progressively reduces further. For example at 160 °C (320 °F) 3 Lect. 8/ Kevlar fibers 3rd class/polymer dep. about 10% reduction in strength occurs after 500 hours. At 260 °C (500 °F) 50% strength reduction occurs after 70 hours.[15] Glass wool This article is about the thermal insulation material composed of glass fibers bonded loosely in a way to trap air. For the plastic composite of glass fiber and polymer plastic used as structural reinforcement, see fiberglass. For the glass fiber itself, also sometimes called fiberglass, see glass fiber. Fiberglass insulation from a ceiling tile Glass wool batt insulation Fiberglass pipe insulation with ASJ (All Service Jacket) penetrating concrete slab opening about to be firestopped. Intumescent wrap strip is used to seal off where the fiberglass will be consumed by fire. Glass wool is an insulating material made from fibres of glass arranged using a binder into a texture similar to wool. The process traps many small pockets of air between the glass, and these small air pockets result in the thermal insulation properties. Glass wool is produced in rolls or in slabs, with different thermal and mechanical properties. It may also be produced as a material that can be sprayed or applied in place, on the surface to be insulated. 4 Lect. 8/ Kevlar fibers 3rd class/polymer dep. Manufacturing process After the mixture of natural sand and recycled glass at 1,450 °C, the glass that is produced is converted into fibers. It is typically produced in a method similar to making cotton candy, forced through a fine mesh by centripetal force, cooling on contact with the air. The cohesion and mechanical strength of the product is obtained by the presence of a binder that “cements” the fibers together. Ideally, a drop of bonder is placed at each fiber intersection. This fiber mat is then heated to around 200 °C to polymerize the resin and is calendered to give it strength and stability. The final stage involves cutting the wool and packing it in rolls or panels under very high pressure before palletizing the finished product in order to facilitate transport and storage. Uses Glass wool is a thermal insulation that consists of intertwined and flexible glass fibers, which causes it to "package" air, resulting in a low density that can be varied through compression and binder content (as noted above, these air cells are the actual insulator). Glass wool can be a loose fill material, blown into attics, or, together with an active binder sprayed on the underside of structures, sheets and panels that can be used to insulate flat surfaces such as cavity wall insulation, ceiling tiles, curtain walls as well as ducting. It is also used to insulate piping and for soundproofing. Health problems In the US, the National Toxicology Program ("NTP"), in June 2011, removed from its Report on Carcinogens all biosoluble glass wool used in home and building insulation and for non-insulation products.[1] Similarly, California's Office of Environmental Health Hazard Assessment ("OEHHA"), in November 2011, published a modification to its Proposition 65 listing to include only "Glass wool fibers (inhalable and biopersistent)."[2] The U.S. NTP and California's OEHHA action means that a cancer warning label for biosoluble fiber glass home and building insulation is no longer required under Federal or California law. All fiber glass wools commonly used for thermal and acoustical insulation were reclassified by the International Agency for Research on Cancer ("IARC") in October 2001 as Not Classifiable as to carcinogenicity to humans (Group 3).[3] 5 Lect. 8/ Kevlar fibers 3rd class/polymer dep. Fiberglass will irritate the eyes, skin, and the respiratory system. Potential symptoms include irritation of eyes, skin, nose, throat, dyspnea (breathing difficulty); sore throat, hoarseness and cough.[4] Scientific evidence demonstrates that fiber glass is safe to manufacture, install and use when recommended work practices are followed to reduce temporary mechanical irritation.[5] Fiberglass is resistant to mold but growth can occur if fiberglass becomes wet and contaminated with organic material. Fiberglass insulation that has become wet should be inspected for evidence of residual moisture and contamination. Contaminated fiberglass insulation should be promptly removed Wool fibers: 6