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Polymers melting temperatures

Chemical Properties. The hydrolysis of PET is acid- or base-catalyzed and is highly temperature dependent and relatively rapid at polymer melt temperatures. Treatment for several weeks in 70°C water results in no significant fiber strength loss. However, at 100°C, approximately 20% of the PET tenacity is lost in one week and about 60% is lost in three weeks (47). In general, the hydrolysis and chemical resistance of copolyester materials is less than that for PET and depends on both the type and amount of comonomer. [Pg.326]

Polymer Melt temperature i°C) Mould temperature (X) SG Specific heat (Jkg- K ) Heat required to melt Heat removed on cooling ... [Pg.162]

Semicrystalline partial aromatic polyamides, 139 Semicrystalline polyesters, 45 Semicrystalline polymers, melting temperatures of, 33 Semirigid foams, 203 tests for, 244 Sensitization, 246... [Pg.600]

Polymer Melting temperature (°C) Young s modulus (GPa) Tensile strength (MPa) Elongation to break (%) Notched izod impact strength (J/m)... [Pg.269]

To a three-necked, round-bottomed flask equipped with a mechanical stirrer, dropping funnel, and condenser is added a solution of 4.95 gm (0.05 mole) of phosgene in 200 ml of dry carbon tetrachloride. The solution is vigorously stirred while the rapid addition of 5.8 gm (0.05 mole) of hexamethylenediamine and 4.0 gm (0.10 mole) of sodium hydroxide in 70 ml of water takes place. The reaction is exothermic while the polyurea forms. After 10 min, the carbon tetrachloride is evaporated off on a steam bath or with the aid of a water aspirator. The polyurea is washed several times in a blender and air-dried overnight to obtain 5.0 gm (70 %), inherent viscosity 0.90 (in w-cresol, 0.5 % concentration at 30°C), polymer melt temperature approximately 295°C. [Pg.81]

The polymer precipitates immediately and stirring is continued for an additional 5 min. The polymer is filtered, boiled in water for 15 min, filtered, dried under reduced pressure at 70°C to afford a quantitative yield of polymer, inherent viscosity 0.31 (sulfuric acid), polymer melt temperature 306°C. The polymer is soluble in formic acid from which a film can be cast. [Pg.354]

Table 10.1 compares the carrier substances water, nitrogen, and carbon dioxide for the intake of 1 kg of stripping agent at a polymer melt temperature of 200 °C. [Pg.188]

The minimum conditions (partial pressure, temperature) for degassing the volatile components should not be restricted by the maximum allowable polymer melt temperature. The key data for degassing is obtained from the vapor pressure of the volatile components and/or the equilibrium diagrams, which are generally not available for complex or new material systems. [Pg.193]

The mouldability index is the length of the elongated flow path that is filled before solidification of the injected molten polymer composition at specified moulding conditions, i.e., volumetric injection rate, mould temperature, polymer melt temperature. The mouldability index of the moulding compositions of this invention is characterised by spiral flow. [Pg.806]

Fig. 4.8.7. Typical DSC curves of a crystalline polymer melting temperature (T, ), crystallization temperature (7V), glass transition temperature (Tg), and cold crystallization temperature (T )... Fig. 4.8.7. Typical DSC curves of a crystalline polymer melting temperature (T, ), crystallization temperature (7V), glass transition temperature (Tg), and cold crystallization temperature (T )...
Table I shews the effect of BD content on the properties of injection-molded BDA/HD/BD polyesters. The actual polymer melt temperatures during molding were between the temperatures listed... Table I shews the effect of BD content on the properties of injection-molded BDA/HD/BD polyesters. The actual polymer melt temperatures during molding were between the temperatures listed...
As a consequence, together with linear chains, branched and crosslinked structures are also formed. They strongly affect molecular masses, MMD, and solution properties. Moreover, these non-crystal 1izable units cause a decrease of both the polymer melting temperature and the crystallization rate, as well as a poorer thermo-oxidative stability (16). [Pg.171]

Several approaches for producing polyanhydride microspheres were developed. One was a hot-melt technique. This process yielded spherical microspheres, and the capsule yield was almost quantitative. The release of acid orange and insulin from PCPP-SA was studied. This approach is most useful for molecules that are exposed to the polymer melting temperature (76°C) without inactivation (26). [Pg.14]

Figure 1 Relation of polymer melt temperature and composition for a series of copolyazomethlnes from 2-methyl—1,4—phenylene-diamlne, 1,4-phenylenedlamine and terephthalaldehyde. Figure 1 Relation of polymer melt temperature and composition for a series of copolyazomethlnes from 2-methyl—1,4—phenylene-diamlne, 1,4-phenylenedlamine and terephthalaldehyde.
Polymer Melt Temperature Polymer melting was determined on dry, powdered polymer on a chrome-plated gradient temperature bar (14) and Is noted as the temperature at which the polymer under moderate sliding pressure leaves a molten or waxy trail adhering to the bar. [Pg.113]

PIP product improvement program PMT polymer melting temperature... [Pg.608]

Most aromatic polyamides cannot be made by a melt polymerization process because the polymer melt temperature exceeds the decomposition temperature. Singh developed a unique procedure for preparing certain aromatic polyamides by a melt process using an internal plasticizer generated in-situ during the polymerization [82]. The following reaction scheme was used to prepare aromatic polyamides in the absence of a solvent (Equation 13.24). [Pg.1000]

For certain uses, it is desirable to prepare biodegradable PVA plasticized with biodegradable plasticizers that specifically assist in lowering the polymer melt temperature and the extrusion temperature and at the same time maximize water solubility by minimizing crystallinity. A PVA composition has been described that is transesteri-fied with a polyol as plasticizer (16). [Pg.49]


See other pages where Polymers melting temperatures is mentioned: [Pg.130]    [Pg.144]    [Pg.99]    [Pg.79]    [Pg.326]    [Pg.329]    [Pg.22]    [Pg.162]    [Pg.193]    [Pg.27]    [Pg.25]    [Pg.356]    [Pg.102]    [Pg.546]    [Pg.23]    [Pg.69]    [Pg.64]    [Pg.18]    [Pg.271]    [Pg.272]    [Pg.274]    [Pg.276]    [Pg.419]    [Pg.223]    [Pg.319]    [Pg.171]    [Pg.2091]    [Pg.468]    [Pg.41]   
See also in sourсe #XX -- [ Pg.14 , Pg.15 ]

See also in sourсe #XX -- [ Pg.261 , Pg.263 , Pg.270 , Pg.284 , Pg.285 , Pg.287 ]




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Cross-linked polymers equilibrium melting temperature

Crystalline polymers melting temperature

Diene type polymers melting temperatures

Equilibrium melting temperature, of polymer

Equilibrium melting temperature, of polymer crystals

Equilibrium melting temperature, polymer

Equilibrium melting temperature, polymer crystal nucleation

Melted polymer

Melting temperature Melts

Melting temperature of polymer crystals

Melting temperature of polymers

Melting temperature polymer blends

Melting temperature, polymer crystal

Melting temperature, polymer crystal nucleation

Melting-transition temperature polymer heat capacity

Melting-transition temperature polymer thermodynamics, first-order

Polymer high-temperature melting

Polymer melt transition temperature

Polymer melting characteristic temperatures

Polymer melts

Polymer science melt temperature

Polymer science melting temperature

Polymer temperature

Polymer-diluent mixtures melting temperatures

Polymers melting temperature, factors affecting

Pressure-Volume-Temperature Relationship for Polymer Melts

Relationship between glass transition temperature and melting point of polymers

Temperatur melting

Thermodynamic equilibrium melting temperature of polymer crystals

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