Viscosity glass transition temperature

The curing and dynamic properties of precipitated nano-silica on NR without and with the sulfur addition (NR with S), synthetic polyisoprene (IR), polybutadiene (BR) and SBR was investigated. Silica was treated with bis(3-triethoxysilylpropyl)tetrasulfane (TESPT) to form bonds at interfaces. Cure, Mooney viscosity, glass transition temperature, bound rubber, crosslink density and DMA were measured. The properties of silica-filled SBR and BR correlated with highest rolling resistance and SBR-silica correlated with best skid resistance. A Payne effect was observed in the loss modulus under some experimental conditions. In addition to possible filler de-agglomeration and network disruption, the nanoscale of the filler may have further contributed to the non-linear response typified by the Payne effect. ... 

Properties of polyamide-poly(ethylene terephthalate) mixtures have been evaluated with particular reference to viscosity, glass transition temperatures, and thermal stability studies. 

Plasticizers are reducing the modulus, tensile strength, hardness, density, melt viscosity, glass transition temperature, electrostatic chargeability and volume resistivity of a polymer. In contrast, they are increasing the flexibility, elongation at break, toughness, dielectric constant and power factor (2). 

Hampshire, S., Drew, R. A. L., Jack, K. H. (1984). Viscosities, glass-transition temperatures, and microhardness of Y-Si-Al-O-N glasses. Journal of the American Ceramic Society, 67(3), C46-C47. 

In addition to thermodynamic appUcations, 62 values have also been related to the glass transition temperature of a polymer, and the difference 62-61 to the viscosity of polymer solutions. The best values of 6 have been analyzed into group contributions, the sum of which can be used to estimate 62 for polymers which have not been characterized experimentally. 

Solution Polymers. Acryflc solution polymers are usually characterized by their composition, solids content, viscosity, molecular weight, glass-transition temperature, and solvent. The compositions of acryflc polymers are most readily determined by physicochemical methods such as spectroscopy, pyrolytic gas—liquid chromatography, and refractive index measurements (97,158). The solids content of acryflc polymers is determined by dilution followed by solvent evaporation to constant weight. Viscosities are most conveniently determined with a Brookfield viscometer, molecular weight by intrinsic viscosity (158), and glass-transition temperature by calorimetry. 

The iatroduction of a plasticizer, which is a molecule of lower molecular weight than the resia, has the abiUty to impart a greater free volume per volume of material because there is an iucrease iu the proportion of end groups and the plasticizer has a glass-transition temperature, T, lower than that of the resia itself A detailed mathematical treatment (2) of this phenomenon can be carried out to explain the success of some plasticizers and the failure of others. Clearly, the use of a given plasticizer iu a certain appHcation is a compromise between the above ideas and physical properties such as volatiUty, compatibihty, high and low temperature performance, viscosity, etc. This choice is appHcation dependent, ie, there is no ideal plasticizer for every appHcation. 

Since successful commercialization of Kapton by Du Pont Company in the 1960s (10), numerous compositions of polyimide and various new methods of syntheses have been described in the Hterature (1—5). A successful result for each method depends on the nature of the chemical components involved in the system, including monomers, intermediates, solvents, and the polyimide products, as well as on physical conditions during the synthesis. Properties such as monomer reactivity and solubiHty, and the glass-transition temperature,T, crystallinity, T, and melt viscosity of the polyimide products ultimately determine the effectiveness of each process. Accordingly, proper selection of synthetic method is often critical for preparation of polyimides of a given chemical composition. 

The Arrhenius equation holds for many solutions and for polymer melts well above their glass-transition temperatures. For polymers closer to their T and for concentrated polymer and oligomer solutions, the WiUiams-Landel-Ferry (WLF) equation (24) works better (25,26). With a proper choice of reference temperature T, the ratio of the viscosity to the viscosity at the reference temperature can be expressed as a single universal equation (eq. 8) ... 

Plasticizers and Processing Aids. Petroleum-based oils are commonly used as plasticizers. Compound viscosity is reduced, and mixing, processing, and low temperature properties are improved. Air permeabihty is increased by adding extender oils. Plasticizers are selected for their compatibihty and low temperature properties. Butyl mbber has a solubihty parameter of ca 15.3 (f /cm ) [7.5 (cal/cm ) ], similar to paraffinic and naphthenic oils. Polybutenes, paraffin waxes, and low mol wt polyethylene can also be used as plasticizers (qv). Alkyl adipates and sebacates reduce the glass-transition temperature and improve low temperature properties. Process aids, eg, mineral mbber and Stmktol 40 ms, improve filler dispersion and cured adhesion to high unsaturated mbber substrates. 

As the temperature is decreased, free-volume is lost. If the molecular shape or cross-linking prevent crystallisation, then the liquid structure is retained, and free-volume is not all lost immediately (Fig. 22.8c). As with the melt, flow can still occur, though naturally it is more difficult, so the viscosity increases. As the polymer is cooled further, more free volume is lost. There comes a point at which the volume, though sufficient to contain the molecules, is too small to allow them to move and rearrange. All the free volume is gone, and the curve of specific volume flattens out (Fig. 22.8c). This is the glass transition temperature, T . Below this temperature the polymer is a glass. 

If we, however, consider that viscosity is inversely related to the fractional free volume, which increases from a small value at the glass transition temperature Tg linearly with temperature above this figure, then it is possible to derive an equation. 

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. 

SBR latices are high-solids dispersions of rubber particles in water, the viscosity and rheology of which are, in general, independent of the polymer properties, unlike solutions. They offer a wide range of molecular weight and glass transition temperature. Three classes of SBR latices are available in the market. 

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