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Thermal properties heat expansion coefficients

In order to select materials that will maintain acceptable mechanical characteristics and dimensional stability one must be aware of both the normal and extreme thermal operating environments to which a product will be subjected. TS plastics have specific thermal conditions when compared to TPs that have various factors to consider which influence the product s performance and processing capabilities. TPs properties and processes are influenced by their thermal characteristics such as melt temperature (Tm), glass-transition temperature (Tg), dimensional stability, thermal conductivity, specific heat, thermal diffusivity, heat capacity, coefficient of thermal expansion, and decomposition (Td) Table 1.2 also provides some of these data on different plastics. There is a maximum temperature or, to be more precise, a maximum time-to-temperature relationship for all materials preceding loss of performance or decomposition. Data presented for different plastics in Figure 1.5 show 50% retention of mechanical and physical properties obtainable at room temperature, with plastics exposure and testing at elevated temperatures. [Pg.17]

In recent years, the concept of light construction has led to the development of hybrid structural parts. Using parts made of pure plastic runs into repeated difficulties because of the material s low modulus of elasticity, since the only way to compensate for this drawback is to use much thicker structures. Combinations of sheet metal materials with plastics facilitate new solutions that do justice to the concept of lightweight construction and provide new properties at the same time (sound insulation, thermal conductivity, dynamic stability, corrosion protection). The precondition for successful development of such hybrid structural parts is a reliable bond between the two materials. In certain cases, this must be realized by adhesives that are flexible with regard to the a problem (different heat expansion coefficients of the materials), but still provide high strength levels. [Pg.217]

In Older to calculate the temperature distribution and the thermal stress distribution in the FGM cylinder, effective material properties such as heat expansion coefficient a(r), heat conduct on coefficient k(r), the volume modulus K(r), the shear elasticity G(r) and Young s modi u., E(r) for intermediate composition of the FGM are required. This paper assumes that. ach layer of FGM is simple macroscopicaUy isotropic two-phase system with spherical particles.We utilize formula proposed by K.WakashimaWto calculate effective properties in each layer. [Pg.37]

Thermal decompositions have been studied most effectively by mass spectroscopic thermal analysis, thermogravimetric analysis, and electrical conductivity. Several analytical characterizations of phenolic resins have recently been reported, making use of a variety of properties, including expansion coefficients, " specific heat capacity, ultrasonic properties, dipole moments, and laser light scattering. Recently, high-temperature properties of reinforced phenolic components have been studied by Goetzel. ... [Pg.91]

Material Properties. The properties of materials are ultimately deterrnined by the physics of their microstmcture. For engineering appHcations, however, materials are characterized by various macroscopic physical and mechanical properties. Among the former, the thermal properties of materials, including melting temperature, thermal conductivity, specific heat, and coefficient of thermal expansion, are particularly important in welding. [Pg.346]

Thermal Properties. Thermal properties include heat-deflection temperature (HDT), specific heat, continuous use temperature, thermal conductivity, coefficient of thermal expansion, and flammability ratings. Heat-deflection temperature is a measure of the minimum temperature that results in a specified deformation of a plastic beam under loads of 1.82 or 0.46 N/mm (264 or 67 psi, respectively). Eor an unreinforced plastic, this is typically ca 20°C below the glass-transition temperature, T, at which the molecular mobility is altered. Sometimes confused with HDT is the UL Thermal Index, which Underwriters Laboratories estabflshed as a safe continuous operation temperature for apparatus made of plastics (37). Typically, UL temperature indexes are significantly lower than HDTs. Specific heat and thermal conductivity relate to insulating properties. The coefficient of thermal expansion is an important component of mold shrinkage and must be considered when designing composite stmctures. [Pg.264]

Thermal Properties at Low Temperatures For sohds, the Debye model developed with the aid of statistical mechanics and quantum theoiy gives a satisfactoiy representation of the specific heat with temperature. Procedures for calculating values of d, ihe Debye characteristic temperature, using either elastic constants, the compressibility, the melting point, or the temperature dependence of the expansion coefficient are outlined by Barron (Cryogenic Systems, 2d ed., Oxford University Press, 1985, pp 24-29). [Pg.1127]

The resin is too brittle to give a tme meaning to mechanical properties. The thermal properties are interesting in that there appears to be a transition point at 46°C. Above this temperature, specific heat and temperature coefficient of expansion are much greater than below it. The specific heat of hardened shellac at 50°C is lower than that of unhardened material, this no doubt reflecting the disappearance, or at least the elevation, of the transition temperature. [Pg.869]

The transition between crystalline and amorphous polymers is characterized by the so-called glass transition temperature, Tg. This important quantity is defined as the temperature above which the polymer chains have acquired sufficient thermal energy for rotational or torsional oscillations to occur about the majority of bonds in the chain. Below 7"g, the polymer chain has a more or less fixed conformation. On heating through the temperature Tg, there is an abrupt change of the coefficient of thermal expansion (or), compressibility, specific heat, diffusion coefficient, solubility of gases, refractive index, and many other properties including the chemical reactivity. [Pg.140]

Several material properties exhibit a distinct change over the range of Tg. These properties can be classified into three major categories—thermodynamic quantities (i.e., enthalpy, heat capacity, volume, and thermal expansion coefficient), molecular dynamics quantities (i.e., rotational and translational mobility), and physicochemical properties (i.e., viscosity, viscoelastic proprieties, dielectric constant). Figure 34 schematically illustrates changes in selected material properties (free volume, thermal expansion coefficient, enthalpy, heat capacity, viscosity, and dielectric constant) as functions of temperature over the range of Tg. A number of analytical methods can be used to monitor these and other property changes and... [Pg.72]

LIG. 34 Schematic illustrations of changes in selected material properties (free volume, thermal expansion coefficient, enthalpy, heat capacity, viscosity, and dielectric constant) as functions of temperature over the range of Tg. [Pg.73]

The principal thermal properties of importance in the present context are specific heat, thermal conductivity, coefficient of expansion and stability. [Pg.86]

Gases, partial derivatives, triangle relation, inverse relation, total differential Properties (Heat capacity, thermal expansion coefficient, isothermal expansivity coefficient)... [Pg.297]

Glass transition temperature is one of the most important parameters used to determine the application scope of a polymeric material. Properties of PVDF such as modulus, thermal expansion coefficient, dielectric constant and loss, heat capacity, refractive index, and hardness change drastically helow and above the glass transition temperature. A compatible polymer blend has properties intermediate between those of its constituents. The change of glass transition temperature has been a widely used method to study the compatibility of polymer blends. Normally, the glass transition temperatme of a compatible polymer blend can be predicted by the Gordon-Taylor relation ... [Pg.122]

The state of polarization, and hence the electrical properties, responds to changes in temperature in several ways. Within the Bom-Oppenheimer approximation, the motion of electrons and atoms can be decoupled, and the atomic motions in the crystalline solid treated as thermally activated vibrations. These atomic vibrations give rise to the thermal expansion of the lattice itself, which can be measured independendy. The electronic motions are assumed to be rapidly equilibrated in the state defined by the temperature and electric field. At lower temperatures, the quantization of vibrational states can be significant, as manifested in such properties as thermal expansion and heat capacity. In polymer crystals quantum mechanical effects can be important even at room temperature. For example, the magnitude of the negative axial thermal expansion coefficient in polyethylene is a direct result of the quantum mechanical nature of the heat capacity at room temperature." At still higher temperatures, near a phase transition, e.g., the assumption of stricdy vibrational dynamics of atoms is no... [Pg.193]

The approach to the critical point, from above or below, is accompanied by spectacular changes in optical, thermal, and mechanical properties. These include critical opalescence (a bright milky shimmering flash, as incident light refracts through intense density fluctuations) and infinite values of heat capacity, thermal expansion coefficient aP, isothermal compressibility /3r, and other properties. Truly, such a confused state of matter finds itself at a critical juncture as it transforms spontaneously from a uniform and isotropic form to a symmetry-broken (nonuniform and anisotropically separated) pair of distinct phases as (Tc, Pc) is approached from above. Similarly, as (Tc, Pc) is approached from below along the L + G coexistence line, the densities and other phase properties are forced to become identical, erasing what appears to be a fundamental physical distinction between liquid and gas at all lower temperatures and pressures. [Pg.49]


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