Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nylon 6,6, melting point

Nylon Melting Point (°C) Nylon Melting Point (°C)... [Pg.108]

Thermoplastic Fibers. The thermoplastic fibers, eg, polyester and nylon, are considered less flammable than natural fibers. They possess a relatively low melting point furthermore, the melt drips rather than remaining to propagate the flame when the source of ignition is removed. Most common synthetic fibers have low melting points. Reported values for polyester and nylon are 255—290°C and 210—260°C, respectively. [Pg.490]

Many polymers, including polyethylene, polypropylene, and nylons, do not dissolve in suitable casting solvents. In the laboratory, membranes can be made from such polymers by melt pressing, in which the polymer is sandwiched at high pressure between two heated plates. A pressure of 13.8—34.5 MPa (2000—5000 psi) is appHed for 0.5 to 5 minutes, at a plate temperature just above the melting point of the polymer. Melt forming is commonly used to make dense films for packaging appHcations, either by extmsion as a sheet from a die or as blown film. [Pg.62]

Fig. 5. The dependence of remanent polarization, P, on the melting point, T, in odd nylons (40). Fig. 5. The dependence of remanent polarization, P, on the melting point, T, in odd nylons (40).
Polymer Production. Three processes are used to produce nylon-6,6. Two of these start with nylon-6,6 salt, a combination of adipic acid and hexamethylenediamine in water they are the batch or autoclave process and the continuous polymerisation process. The third, the soHd-phase polymerisation process, starts with low molecular weight pellets usually made via the autoclave process, and continues to build the molecular weight of the polymer in a heated inert gas, the temperature of which never reaches the melting point of the polymer. [Pg.233]

Nylon-11. Nylon-11 [25035-04-5] made by the polycondensation of 11-aminoundecanoic acid [2432-99-7] was first prepared by Carothers in 1935 but was first produced commercially in 1955 in France under the trade name Kilsan (167) Kilsan is a registered trademark of Elf Atochem Company. The polymer is prepared in a continuous process using phosphoric or hypophosphoric acid as a catalyst under inert atmosphere at ambient pressure. The total extractable content is low (0.5%) compared to nylon-6 (168). The polymer is hydrophobic, with a low melt point (T = 190° C), and has excellent electrical insulating properties. The effect of formic acid on the swelling behavior of nylon-11 has been studied (169), and such a treatment is claimed to produce a hard elastic fiber (170). [Pg.236]

Nylon-12,12. Nylon-12,12 [36497-34-4] [36348-71-7] was introduced into the marketplace by Du Pont in the late 1980s (174). This polymer possesses very low moisture absorption, high dimensional stabihty, and excellent chemical resistance, with a moderately high melt point (T = 185° C)... [Pg.236]

The pelargonic acid by-product is already a useful item of commerce, making the overall process a commercial possibiUty. The 13-carbon polyamides appear to have many of the properties of nylon-11, nylon-12, or nylon-12,12 toughness, moisture resistance, dimensional stabiUty, increased resistance to hydrolysis, moderate melt point, and melt processibiUty. Thus, these nylons could be useful in similar markets, eg, automotive parts, coatings, fibers, or films. Properties for nylon-13,13 are = 56 (7 and = 183 (7 (179). [Pg.237]

Fig. 10. Effect on melting point of varying composition of nylon-6,6 and nylon-6, where A represents a physical blend, and B, an equiUbrated random... Fig. 10. Effect on melting point of varying composition of nylon-6,6 and nylon-6, where A represents a physical blend, and B, an equiUbrated random...
Fig. 17. Melting point—composition curves for random copolyamides of nylon-6,6. Fig. 17. Melting point—composition curves for random copolyamides of nylon-6,6.
The thermoplastic or thermoset nature of the resin in the colorant—resin matrix is also important. For thermoplastics, the polymerisation reaction is completed, the materials are processed at or close to their melting points, and scrap may be reground and remolded, eg, polyethylene, propjiene, poly(vinyl chloride), acetal resins (qv), acryhcs, ABS, nylons, ceUulosics, and polystyrene (see Olefin polymers Vinyl polymers Acrylic ester polymers Polyamides Cellulose ESTERS Styrene polymers). In the case of thermoset resins, the chemical reaction is only partially complete when the colorants are added and is concluded when the resin is molded. The result is a nonmeltable cross-linked resin that caimot be reworked, eg, epoxy resins (qv), urea—formaldehyde, melamine—formaldehyde, phenoHcs, and thermoset polyesters (qv) (see Amino resins and plastics Phenolic resins). [Pg.456]

The nylon 66 salt is prepared by reacting the hexamethylenediamine and adipic acid in boiling methanol, the comparatively insoluble salt (melting point 190-191°C) precipitating out. [Pg.486]

The glass transition temperatures of the nylons appear to be below room temperature so that the materials have a measure of flexibility in spite of their high crystallinity under general conditions of service. The polymers have fairly sharply defined melting points and above this temperature the homopolymers have low melt viscosities. Some thermal properties of the nylons are given in Table 18.4. [Pg.493]

In addition to the nucleating agents discussed in Section 18.4, many other materials have been found to be effective. Whilst the nylons may be self-nucleating, partieularly if there is some unmelted crystal structure, seeding with higher melting point polymers can be effective. Thus nylon 66 and poly(ethylene terephthalate) are reported to be especially attractive for nylon 6. [Pg.497]

The particular features of the nylons should also be taken into account in extrusion. Dry granules must be used unless a devolatilising extruder is employed. Because of the sharp melting point it is found appropriate to use a screw with a very short compression zone. Polymers of the lowest melt viscosity are to be avoided since they are difficult to handle. Provision should be made to initiate cooling immediately the extrudate leaves the die. [Pg.501]


See other pages where Nylon 6,6, melting point is mentioned: [Pg.172]    [Pg.172]    [Pg.172]    [Pg.172]    [Pg.68]    [Pg.171]    [Pg.219]    [Pg.220]    [Pg.222]    [Pg.223]    [Pg.224]    [Pg.235]    [Pg.236]    [Pg.236]    [Pg.237]    [Pg.237]    [Pg.237]    [Pg.238]    [Pg.238]    [Pg.239]    [Pg.240]    [Pg.246]    [Pg.246]    [Pg.259]    [Pg.267]    [Pg.267]    [Pg.267]    [Pg.269]    [Pg.273]    [Pg.299]    [Pg.64]    [Pg.267]    [Pg.52]    [Pg.486]    [Pg.488]    [Pg.507]    [Pg.718]   
See also in sourсe #XX -- [ Pg.135 ]




SEARCH



Nylon melt

© 2024 chempedia.info