Nylon-6,6 Poly

Preparation of poly(nylon-6-block-diethyleneglycol terephthalate)... 

The production of polyester fibers leads that of all other types Annual United States production of poly ester fibers is 1 6 million tons versus 1 4 million tons for cotton and 1 0 million tons for nylon Wool and silk trail far behind at 0 04 and 0 01 million tons re spectively... 

Properties Nylon 6/9, molding and extrusion Nylon 6/12 Nylon 11, molding and extrusion Nylon 12, molding and extrusion Aromatic nylon (aramid), molded and unfilled Poly(amide- imide), unfilled... 

The polyamides poly(hexamethylene sebacamide) and poly(hexamethylene adipamide) are also widely known as nylon-6,10 and nylon-6,6, respectively. The numbers following the word nylon indicate the number of carbon atoms in the diamine and dicarboxylic acid, in that order. On the basis of this same system, poly (e-caprolactam) is also known as nylon-6. 

Nylon-6,6 cord Poly (ethylene terephthalate) cord ... 

Poly[imino(l,d-dioxo-hexanediyl)imino-hexanediyl]. See Nylon-d,d. 

Most of the polymer s characteristics stem from its molecular stmcture, which like POE, promotes solubiUty in a variety of solvents in addition to water. It exhibits Newtonian rheology and is mechanically stable relative to other thermoplastics. It also forms miscible blends with a variety of other polymers. The water solubiUty and hot meltable characteristics promote adhesion in a number of appHcations. PEOX has been observed to promote adhesion comparable with PVP and PVA on aluminum foil, cellophane, nylon, poly(methyl methacrylate), and poly(ethylene terephthalate), and in composite systems improved tensile strength and Izod impact properties have been noted. 

However, because of the low melting poiats and poor hydrolytic stabiUty of polyesters from available iatermediates, Carothers shifted his attention to linear ahphatic polyamides and created nylon as the first commercial synthetic fiber. It was nearly 10 years before. R. Whinfield and J. T. Dickson were to discover the merits of poly(ethylene terephthalate) [25038-59-9] (PET) made from aromatic terephthaUc acid [100-21-0] (TA) and ethylene glycol [107-21-1] (2G). 

Chemical Concen-trati T emper- ature. Time, h Kuralon Cotton Nylon Poly-e... 

The film tube is collapsed within a V-shaped frame of rollers and is nipped at the end of the frame to trap the air within the bubble. The nip roUs also draw the film away from the die. The draw rate is controlled to balance the physical properties with the transverse properties achieved by the blow draw ratio. The tube may be wound as such or may be sHt and wound as a single-film layer onto one or more roUs. The tube may also be direcdy processed into bags. The blown film method is used principally to produce polyethylene film. It has occasionally been used for polypropylene, poly(ethylene terephthalate), vinyls, nylon, and other polymers. 

The Fe, Co, and Ni deposits are extremely fine grained at high current density and pH. Electroless nickel, cobalt, and nickel—cobalt alloy plating from fluoroborate-containing baths yields a deposit of superior corrosion resistance, low stress, and excellent hardenabiUty (114). Lead is plated alone or ia combination with tin, iadium, and antimony (115). Sound iasulators are made as lead—plastic laminates by electrolyticaHy coating Pb from a fluoroborate bath to 0.5 mm on a copper-coated nylon or polypropylene film (116) (see Insulation, acoustic). Steel plates can be simultaneously electrocoated with lead and poly(tetrafluoroethylene) (117). Solder is plated ia solutioas containing Pb(Bp4)2 and Sn(Bp4)2 thus the lustrous solder-plated object is coated with a Pb—Sn alloy (118). 

In 1954 the surface fluorination of polyethylene sheets by using a soHd CO2 cooled heat sink was patented (44). Later patents covered the fluorination of PVC (45) and polyethylene bottles (46). Studies of surface fluorination of polymer films have been reported (47). The fluorination of polyethylene powder was described (48) as a fiery intense reaction, which was finally controlled by dilution with an inert gas at reduced pressures. Direct fluorination of polymers was achieved in 1970 (8,49). More recently, surface fluorinations of poly(vinyl fluoride), polycarbonates, polystyrene, and poly(methyl methacrylate), and the surface fluorination of containers have been described (50,51). Partially fluorinated poly(ethylene terephthalate) and polyamides such as nylon have excellent soil release properties as well as high wettabiUty (52,53). The most advanced direct fluorination technology in the area of single-compound synthesis and synthesis of high performance fluids is currently practiced by 3M Co. of St. Paul, Minnesota, and by Exfluor Research Corp. of Austin, Texas. 

Poly(vinylidene chloride). Poly(viayHdene chloride) [9002-85-1] (PVDC), most of which is produced by Dow Chemical, is best known in its saran or PVC-copolymerized form (see Vinylidene chloride and poly(VINYLIDENE chloride)). As solvent or emulsion coating, PVDC imparts high oxygen, fat, aroma, and water-vapor resistance to substrates such as ceUophane, oriented polypropylene, polyester, and nylon. 

In the second quarter of the twentieth century, with the development of poly(vinyl chloride), nylon, polyurethane, and other polymers, many new and improved leather-like materials, so-called coated fabrics (qv), were placed on the market. Shortages of leather after World War 11 led to the expansion of these leather-like materials ("man-made" leathers) to replace leather in shoes, clothing, bags, upholstery, and other items. DurabiUty and waterproof quahties superior to leather made coated fabrics advantageous, in spite of imperfection in breathabihty and flexibiUty. Demands for shoes, clothing, and other items are stiU increasing due to growing world population and urbanization. 

Membrane Sep r tion. The separation of components ofhquid milk products can be accompHshed with semipermeable membranes by either ultrafiltration (qv) or hyperfiltration, also called reverse osmosis (qv) (30). With ultrafiltration (UF) the membrane selectively prevents the passage of large molecules such as protein. In reverse osmosis (RO) different small, low molecular weight molecules are separated. Both procedures require that pressure be maintained and that the energy needed is a cost item. The materials from which the membranes are made are similar for both processes and include cellulose acetate, poly(vinyl chloride), poly(vinyHdene diduoride), nylon, and polyamide (see AFembrane technology). Membranes are commonly used for the concentration of whey and milk for cheesemaking (31). For example, membranes with 100 and 200 p.m are used to obtain a 4 1 reduction of skimmed milk. 

The packaging (qv) requirements for shipping and storage of thermoplastic resins depend on the moisture that can be absorbed by the resin and its effect when the material is heated to processing temperatures. Excess moisture may result in undesirable degradation during melt processing and inferior properties. Condensation polymers such as nylons and polyesters need to be specially predried to very low moisture levels (3,4), ie, less than 0.2% for nylon-6,6 and as low as 0.005% for poly(ethylene terephthalate) which hydrolyzes faster. 

Because the rules for organic nomenclature determine the priority of naming different carbon chains from their relative lengths, the systematic names for type AABB polyamides depend on the relative length of the carbon chains between the amide nitrogens and the two carbonyl functions of the polymer for aUphatic nylon-Ayy, when x < the lUPAC name is poly[imino-R imino(l2y-dioxo-R )]. When x > then the name is... 

Fig. 4. The effect of temperature on the pie2oelectric strain constant, for A, nylon-11 B, nylon-7 and C, poly(vinyhdene fluoride) (PVF2) films (35).

Polymer Blends. Commercial blends of nylon with other polymers have also been produced in order to obtain a balance of the properties of the two materials or to reduce moisture uptake. Blends of nylon-6,6 with poly(phenylene oxide) have been most successflil, but blends of nylon-6,6 and nylon-6 with polypropylene have also been introduced. 

Blends with good mechanical properties can be made from DMPPO and polymers with which DMPPO is incompatible if an appropriate additive, compatibilizing agent, or treatment is used to increase the dispersion of the two phases. Such blends include mixtures of DMPPO with nylon, polycarbonate, polyester, ABS, and poly(phenylene sulfide). 

Polymer Blends. The miscibility of poly(ethylene oxide) with a number of other polymers has been studied, eg, with poly (methyl methacrylate) (18—23), poly(vinyl acetate) (24—27), polyvinylpyrroHdinone (28), nylon (29), poly(vinyl alcohol) (30), phenoxy resins (31), cellulose (32), cellulose ethers (33), poly(vinyl chloride) (34), poly(lactic acid) (35), poly(hydroxybutyrate) (36), poly(acryhc acid) (37), polypropylene (38), and polyethylene (39). 

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