Dielectric constant/heating

Some physical properties of water are shown in Table 7.2. Water has higher melting and boiling temperatures, surface tension, dielectric constant, heat capacity, thermal conductivity and heats of phase transition than similar molecules (Table 7.3). Water has a lower density than would be expected from comparison with the above molecules and has the unusual property of expansion on solidification. The thermal conductivity of ice is approximately four times greater than that of water at the same temperature and is high compared with other non-metallic solids. Likewise, the thermal dif-fusivity of ice is about nine times greater than that of water. 

The initiation step could also be positively affected by the above-mentioned transport properties, as the efficiency factor f assumes higher values with respect to conventional liquid solvents due to the diminished solvent cage effect One further advantage is constituted by the tunability of the compressibility-dependent properties such as density, dielectric constant, heat capacity, and viscosity, all of which offer additional possibilities to modify the performances of the polymerization process. This aspect could be particularly relevant in the case of copolymerization reactions, where the reactivity ratios of the two monomers, and ultimately the final composition of the copolymer, could be controlled by modifying the pressure of the reaction system. 

To obtain the adsorbed amount as a function of pressure and temperature different variables can be measured adsorbed mass by means of a bedance, consumption of the sorptive gas by means of calibrated volumes, concentration changes in a carrier gas by means of gas chromatography, changes of the dielectric constant, heat of adsorption, nuclear magnetic resonance of special adsorptives, radiation dose of radioactive labelled gas. 

In some cases particles have been added to electrical systems to improve heat removal, for example with an SF -fluidized particulate bed to be used in transformers (47). This process appears feasible, using polytetrafluoroethylene (PTFE) particles of low dielectric constant. For a successful appHcation, practical problems such as fluidizing narrow gaps must be solved. 

Heat treatment of related glasses melted under reducing conditions can yield a unique microfoamed material, or "gas-ceramic" (29). These materials consist of a matrix of BPO glass-ceramic filled with uniformly dispersed 1—10 p.m hydrogen-filled bubbles. The hydrogen evolves on ceranarning, most likely due to a redox reaction involving phosphite and hydroxyl ions. These materials can have densities as low as 0.5 g/cm and dielectric constants as low as 2. 

Material Thermal CTE, ppm/°C Heat capacity. Dielectric constant at 1 Dielectric... 

Commonly used materials for cable insulation are poly(vinyl chloride) (PVC) compounds, polyamides, polyethylenes, polypropylenes, polyurethanes, and fluoropolymers. PVC compounds possess high dielectric and mechanical strength, flexibiUty, and resistance to flame, water, and abrasion. Polyethylene and polypropylene are used for high speed appHcations that require a low dielectric constant and low loss tangent. At low temperatures, these materials are stiff but bendable without breaking. They are also resistant to moisture, chemical attack, heat, and abrasion. Table 14 gives the mechanical and electrical properties of materials used for cable insulation. 

The dielectric constants of amino acid solutions are very high. Thek ionic dipolar structures confer special vibrational spectra (Raman, k), as well as characteristic properties (specific volumes, specific heats, electrostriction) (34). 

Progressive chlorination of a hydrocarbon molecule yields a succession of Hquids and/or soHds of increasing nonflammability, density, and viscosity, as well as improved solubiUty for a large number of inorganic and organic materials. Other physical properties such as specific heat, dielectric constant, and water solubihty decrease with increasing chlorine content. 

The dielectric constant is also affected by stmctural changes on strong heating. Also the value is very rank dependent, exhibiting a minimum at about 88 wt % C and rising rapidly for carbon contents over 90 wt % (4,6,45). Polar functional groups are primarily responsible for the dielectric of lower ranks. For higher ranks the dielectric constant arises from the increase in electrical conductivity. Information on the freedom of motion of the different water molecules in the particles can be obtained from dielectric constant studies (45). 

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