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Physical Properties of Liquids

Table 6. Physical Properties of Liquid Phthalic Anhydride... Table 6. Physical Properties of Liquid Phthalic Anhydride...
Contact manufacturer for final recommendations, give complete system requirements, and physical properties of liquid. Figure 3-69 is convenient for this purpose. [Pg.221]

Tables 23-26 show the variation with temperature of some relevant physical properties of liquid sodium. Tables 23-26 show the variation with temperature of some relevant physical properties of liquid sodium.
General reviews of the structure and properties of liquid crystals can be found in the following G. H. Brown, J. W. Doane, and V. D. Neff. "A Review of the Structure and Physical Properties of Liquid Crystals." CRC Press, Cleveland, Ohio, 1971 P. J. Collings and M. Hind, Introduction to Liquid Crystals. Nature s Delicate Phase of Matter," Taylor and Francis, Inc., Bristol. Pennsylvania, 1997 P. J. Collins, "Liquid Crystals. Nature s Delicate Phase of Matter," Princeton University Press. Princeton. New Jersey, 1990. A thermodynamic description of the phase properties of liquid crystals can be found in S. Kumar, editor, "Liquid Crystals in the Nineties and Beyond, World Scientific, Riven Edge, New Jersey, 1995. [Pg.36]

We have to refine our atomic and molecular model of matter to see how bulk properties can be interpreted in terms of the properties of individual molecules, such as their size, shape, and polarity. We begin by exploring intermolecular forces, the forces between molecules, as distinct from the forces responsible for the formation of chemical bonds between atoms. Then we consider how intermolecular forces determine the physical properties of liquids and the structures and physical properties of solids. [Pg.299]

The same data on physical properties of liquid refrigerants R-N (R-11, R-12, R-13, R-21, R-22, R-113) and their vapor are presented in Tables 7.3-7.8. The detailed data on thermophysical properties of different refrigerants (density, enthalpy, heat capacity, viscosity, thermal conductivity and diffusivity) are found in books by Platzer et al. (1990), Andersen (1959), and Danilova et al. (1976). [Pg.341]

Clearly, then, the chemical and physical properties of liquid interfaces represent a significant interdisciplinary research area for a broad range of investigators, such as those who have contributed to this book. The chapters are organized into three parts. The first deals with the chemical and physical structure of oil-water interfaces and membrane surfaces. Eighteen chapters present discussion of interfacial potentials, ion solvation, electrostatic instabilities in double layers, theory of adsorption, nonlinear optics, interfacial kinetics, microstructure effects, ultramicroelectrode techniques, catalysis, and extraction. [Pg.9]

Effect of physical properties Physical properties of liquid metals that have significant effects on CHF values are thermal conductivity, latent heat of vaporization, and surf ace tension. [Pg.131]

Table 6.2 Approximate physical properties of liquid fuels from various sources [4]... Table 6.2 Approximate physical properties of liquid fuels from various sources [4]...
Comparison of physical properties of liquids, gases and supercritical fluids... [Pg.565]

In many atomization processes, physical phenomena involved have not yet been understood to such an extent that mean droplet size could be expressed with equations derived directly from first principles, although some attempts have been made to predict droplet size and velocity distributions in sprays through maximum entropy principle.I252 432] Therefore, the correlations proposed by numerous studies on droplet size distributions are mainly empirical in nature. However, the empirical correlations prove to be a practical way to determine droplet sizes from process parameters and relevant physical properties of liquid and gas involved. In addition, these previous studies have provided insightful information about the effects of process parameters and material properties on droplet sizes. [Pg.253]

Various correlations for mean droplet size generated by plain-jet, prefilming, and miscellaneous air-blast atomizers using air as atomization gas are listed in Tables 4.7, 4.8, 4.9, and 4.10, respectively. In these correlations, ALR is the mass flow rate ratio of air to liquid, ALR = mAlmL, Dp is the prefilmer diameter, Dh is the hydraulic mean diameter of air exit duct, vr is the kinematic viscosity ratio relative to water, a is the radial distance from cup lip, DL is the diameter of cup at lip, Up is the cup peripheral velocity, Ur is the air to liquid velocity ratio defined as U=UAIUp, Lw is the diameter of wetted periphery between air and liquid streams, Aa is the flow area of atomizing air stream, m is a power index, PA is the pressure of air, and B is a composite numerical factor. The important parameters influencing the mean droplet size include relative velocity between atomization air/gas and liquid, mass flow rate ratio of air to liquid, physical properties of liquid (viscosity, density, surface tension) and air (density), and atomizer geometry as described by nozzle diameter, prefilmer diameter, etc. [Pg.264]

Another important physical property of liquids is the refractive index. Since the refractive index is a constant for a particular liquid at a given temperature, it can be used to help identify substances, check for purity, and measure concentrations. One type of detector found in some liquid chromatograph instruments (Chapter 13) uses refractive index. [Pg.427]

Supercritical fluids possess favorable physical properties that result in good behavior for mass transfer of solutes in a column. Some important physical properties of liquids, gases, and supercritical fluids are compared in Table 4.1 [49]. It can be seen that solute diffusion coefficients are greater in a supercritical fluid than in a liquid phase. When compared to HPLC, higher analyte diffusivity leads to lower mass transfer resistance, which results in sharper peaks. Higher diffusivity also results in higher optimum linear velocities, since the optimum linear velocity for a packed column is proportional to the diffusion coefficient of the mobile phase for liquid-like fluids [50, 51]. [Pg.216]

Table 2.1 Notable Physical Properties of Liquid Water. ... Table 2.1 Notable Physical Properties of Liquid Water. ...
D. Demus, J.W. Goodby, G.W. Gray, H.-W. Speiss and V. Vill (Eds.), Physical Properties of Liquid Crystals, Wiley-VCH, Weinheim, 1999. [Pg.361]

Source T. Lida and R. I. L. Guthrie, The Physical Properties of Liquid Metals. Copyright 1988 Oxford University Press. [Pg.289]

Figure 4.1 Dependence of activation energy for viscous flow on melting point for normal metals and semi-metals. Reprinted, by permission, from T. lida and R. I. L. Guthrie, The Physical Properties of Liquid Metals, p. 187. Copyright 1988 by Oxford University Press. Figure 4.1 Dependence of activation energy for viscous flow on melting point for normal metals and semi-metals. Reprinted, by permission, from T. lida and R. I. L. Guthrie, The Physical Properties of Liquid Metals, p. 187. Copyright 1988 by Oxford University Press.
Physical properties of liquid crystals are generally anisotropic (see, for example, du Jeu, 1980). The anisotropic physical properties that are relevant to display devices are refractive index, dielectric permittivity and orientational elasticity (Raynes, 1983). A nematic LC has two principal refractive indices, Un and measured parallel and perpendicular to the nematic director respectively. The birefringence An = ny — rij is positive, typically around 0.25. The anisotropy in the dielectric permittivity which is given by As = II — Sj is the driving force for most electrooptic effects in LCs. The electric contribution to the free energy contains a term that depends on the angle between the director n and the electric field E and is given by... [Pg.396]

Synthesis and Physical Properties of Liquid Crystals An Interdisciplinary Experiment 118... [Pg.130]

The complexity of the physical properties of liquid water is largely determined by the presence of a three-dimensional hydrogen bond (HB) network [1]. The HB s undergo continuous transformations that occur on ultrafast timescales. The molecular vibrations are especially sensitive to the presence of the HB network. For example, the spectrum of the OH-stretch vibrational mode is substantially broadened and shifted towards lower frequencies if the OH-group is involved in the HB. Therefore, the microscopic structure and the dynamics of water are expected to manifest themselves in the IR vibrational spectrum, and, therefore, can be studied by methods of ultrafast infrared spectroscopy. It has been shown in a number of ultrafast spectroscopic experiments and computer simulations that dephasing dynamics of the OH-stretch vibrations of water molecules in the liquid phase occurs on sub-picosecond timescales [2-14],... [Pg.165]


See other pages where Physical Properties of Liquids is mentioned: [Pg.685]    [Pg.454]    [Pg.424]    [Pg.706]    [Pg.142]    [Pg.464]    [Pg.249]    [Pg.337]    [Pg.565]    [Pg.254]    [Pg.259]    [Pg.263]    [Pg.271]    [Pg.277]    [Pg.91]    [Pg.93]    [Pg.2]    [Pg.354]    [Pg.375]    [Pg.399]    [Pg.304]    [Pg.19]    [Pg.185]   
See also in sourсe #XX -- [ Pg.532 ]




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