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POLYMER CRYSTALL I N I TY. The amorphous nature of polymers is analogous to a plateful of spaghetti --- loose and randomly coiled. T he crystalline state is more like the uncooked spaghetti in the box --- the chains are all tightly bundled and ordered in the same direction.
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POLYMER CRYSTALLINITY • The amorphous nature of polymers is analogous to a plateful of spaghetti --- loose and randomly coiled. • The crystalline state is more like the uncooked spaghetti in the box --- the chains are all tightly bundled and ordered in the same direction.
Electron micrograph of a single crystal of polyethylene The structure of the crystalline regions may be deduced by examination of polymer single crystals, which may be grown from dilute solutions: These crystals are regularly shaped, thin platelets (or lamellae), approximately 10 to 20 nm thick, and on the order of 10 μm long. Frequently, these platelets will form a multilayered structure, like that shown in the electron micrograph of a single crystal of polyethylene.
The chain-folded structure for a plateshaped polymer crystallite. Chain-folded model: The molecular chains within each platelet fold back and forth on themselves,with folds occurring at the faces. Each platelet will consist of a number of polymer molecules.
Many bulk polymers that are crystallized from a melt are semicrystalline and form a spherulite structure. Figure on the left shows the individual chain-folded lamellar crystals that are separated byamorphous material. • Each spherulite may grow to be roughly spherical in shape. • The spherulite consists of ribbon-like chain-folded crystallites (lamellae) that radiate outward from a single nucleation site in the center. • Tie-chain molecules act as connecting links between adjacent lamellae.
Transmission electron micrograph (TEM) showing the spherulite structure in a natural rubber specimen. Chain-folded lamellar crystallites approximately 10 nm thick extend in radial directions from the center; they appear as white thin lines in the micrograph. 30,000X Spherulites are considered to be the polymer analogue of grains in polycrystalline metals and ceramics. However, each spherulite is composed of many different lamellar crystals and, in addition, some amorphous material. PE, PP, PVC, polytetrafluoroethylene, and nylon form a spherulitic structure when they crystallize from a melt.
A transmission photomicrograph (using cross-polarized light) showing the spherulite structure of polyethylene (525X) Linear boundaries form between adjacent spherulites and a characteristic Maltese cross pattern appears within each spherulite.
PET - Poly(ethylene terephthalate) *The polar ester groups make for strong crystals. *In addition, the aromatic rings like to stack together in an orderly fashion, making the crystal even stronger.
Polyketons These polar carbonyl groups are attracted to each other, and very strongly at that. This attraction is so strong that while polyethlyene melts at ~140 °C, the polyketone doesn't melt until 255°C! This makes polyketone very strong but very brittle.
Shell has put the polyketone made with ethylene, carbon monoxide, and a little bit of propylene on the market and sells them under the name Carilon. This polymer is tougher and less brittle.
SRI (nonprofit research institute) International offers Carilon thermoplastic polymers for multiple applications in the engineeringthermoplastic and fiber markets. Originally developed by Shell Oil Company and now available forlicense exclusively through SRI, Carilon polymers offer superior strength, wear and low permeability.These features make them ideal for use in automotive parts; electrical andelectronics systems; business machines and consumer appliances; film, fiber and protective coatings;laboratory supplies, and industrial applications. Representing the next wave in high-performance polymeric materials, Carilon plastics are based ona semicrystalline thermoplastic technology, exhibiting performance characteristics that aremaintained even at high temperatures. Carilon polymers offer a broad range of features: • Outstanding chemical resistance and low permeability • Superior strength, wear and friction characteristics • High resistance to fatigue, creep, swelling and repetitive deformation • Excellent balance of stiffness and toughness over a wide temperature range • High-quality moldings at short cycle times • Resistance to a variety of fuels, organic solvents and aggressive aqueous media • Flame retardancy
Article: Shell Abandons Carilon, Sells Polyurethanes (Company Business and Marketing)(Brief Article) Article from: Chemical Week Article date: February 23, 2000
Kevlar Kevlar is the trademark for a para-aramid synthetic fiber, developed at DuPont in 1965. This high strength material was first commercially used in the early 1970s as a replacement for steel in racing tires. Currently, Kevlar has many applications, ranging from bicycle tires and racing sails to body armor because of its high tensile strength-to-weight ratio; It is 5 times stronger than steel on an equal weight basis.
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