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Temperature normal boiling point

Rebelo, L.RN. et al.. On critical temperature, normal boiling point, and vapor pressures of ionic liquids, ]. Phys. Chem. B, 109, 6040, 2005. [Pg.69]

Rebelo LPN, Canongia Lopes J, Esperanga J et al. (2005) On the critical temperature, normal boiling point, and vapour pressure of ionic liquids. J Phys Chem B 109 6040-6043... [Pg.208]

FIGURE 1.1 Triple Line Temperature, Normal Boiling Point, Critical Temperature, and Surface Tension at the Normal Boiling Point for Several Fluids of Interest. [Pg.4]

Example 9.1 A process involves the use of benzene as a liquid under pressure. The temperature can be varied over a range. Compare the fire and explosion hazards of operating with a liquid process inventory of 1000 kmol at 100 and 150°C based on the theoretical combustion energy resulting from catastrophic failure of the equipment. The normal boiling point of benzene is 80°C, the latent heat of vaporization is 31,000 kJ kmol the specific heat capacity is 150 kJkmoh °C , and the heat of combustion is 3.2 x 10 kJkmok. ... [Pg.269]

Tsup = temperature of the superheated liquid BT = normal boiling point If the mass of liquid vaporized is rriy, then... [Pg.269]

At low temperatures, using the original function/(T ) could lead to greater error. In Tables 4.11 and 4.12, the results obtained by the Soave method are compared with fitted curves published by the DIPPR for hexane and hexadecane. Note that the differences are less than 5% between the normal boiling point and the critical point but that they are greater at low temperature. The original form of the Soave equation should be used with caution when the vapor pressure of the components is less than 0.1 bar. In these conditions, it leads to underestimating the values for equilibrium coefficients for these components. [Pg.157]

Normal boiling point K Standard specific gravity Molecular weight kg/lunol Liquid viscosity at 100°F mm /s Liquid viscosity at 2iO F mm /s Critical temperature K Critical pressure bar... [Pg.416]

The vapour pressure of a liquid increases with rising temperature. A few typical vapour pressure curves are collected in Fig. 7,1, 1. When the vapour pressure becomes equal to the total pressure exerted on the surface of a liquid, the liquid boils, i.e., the liquid is vaporised by bubbles formed within the liquid. When the vapour pressure of the liquid is the same as the external pressure to which the liquid is subjected, the temperature does not, as a rale, rise further. If the supply of heat is increased, the rate at which bubbles are formed is increased and the heat of vaporisation is absorbed. The boiling point of a liquid may be defined as the temperature at which the vapour pressure of the liquid is equal to the external pressure dxerted at any point upon the liquid surface. This external pressure may be exerted by atmospheric air, by other gases, by vapour and air, etc. The boiling point at a pressure of 760 mm. of mercury, or one standard atmosphere, may be termed the normal boiling point. [Pg.2]

As an example of steam distillation, let us consider bromobenzene which has a normal boiling point of 155°. The vapour pressures of water and bromobenzene at different temperature.s are given in the following table. [Pg.14]

The normal boiling point of 2-methylthiazole is 17 0= 128.488 0.005°C. The purity of various thiazoles was determined cryometrically by Handley et al. (292), who measured the precise melting point of thiazole and its monomethyl derivatives. Meyer et al. (293, 294) extended this study and, from the experimental diagrams of crystallization (temperature/degree of crystallization), obtained the true temperatures of crystallization and molar enthalpies of fusion of ideally pure thiazoles (Table 1-43). [Pg.85]

Equations 1 and 2 are easily rearranged to calculate the temperature of the normal boiling point ... [Pg.389]

Titanium is resistant to nitric acid from 65 to 90 wt % and ddute acid below 10 wt %. It is subject to stress—corrosion cracking for concentrations above 90 wt % and, because of the potential for a pyrophoric reaction, is not used in red filming acid service. Tantalum exhibits good corrosion resistance to nitric acid over a wide range of concentrations and temperatures. It is expensive and typically not used in conditions where other materials provide acceptable service. Tantalum is most commonly used in appHcations where the nitric acid is close to or above its normal boiling point. [Pg.45]

Bismuthine. Bismuthine [18288-22-7] BiH, is a colorless gas, unstable at room temperature, but isolatable as a colorless Hquid at lower temperatures. Owing to its instabiUty and difficulty of preparation, no mote than a few hundred milligrams of the pure compound have been available for any single study. Vapot-ptessute data from —116 to —43°C have been determined, and by extrapolation, a normal boiling point of +16.8° C has been indicated AH, calculated from the same data, is 25.15 kj/mol (6.01 kcal/mol) (7). [Pg.127]

Light Olefins and LPG Recovery. Even though the normal boiling point temperature of ethylene (169.4 K) is much above 120 K, its recovery often requites much lower processing temperatures, particularly when high recoveries are needed. [Pg.331]

Helium Purification and Liquefaction. HeHum, which is the lowest-boiling gas, has only 1 degree K difference between its normal boiling point (4.2 K) and its critical temperature (5.2 K), and has no classical triple point (26,27). It exhibits a phase transition at its lambda line (miming from 2.18 K at 5.03 kPa (0.73 psia) to 1.76 K at 3.01 MPa (437 psia)) below which it exhibits superfluid properties (27). [Pg.333]

Properties of Light and Heavy Hydrogen. Vapor pressures from the triple point to the critical point for hydrogen, deuterium, tritium, and the various diatomic combinations are Hsted in Table 1 (15). Data are presented for the equiUbrium and normal states. The equiUbrium state for these substances is the low temperature ortho—para composition existing at 20.39 K, the normal boiling point of normal hydrogen. The normal state is the high (above 200 K) temperature ortho—para composition, which remains essentially constant. [Pg.3]

The normal boiling point of /V-ethylaniline is 204°C. Therefore, steam distillation makes possible the distillation of /V-ethylaniline at atmospheric pressure at a temperature of 99.15°C instead of its normal boiling point of 204°C. Commercial appHcations of steam distillation include the fractionation of cmde tall oil (qv) (84), the distilling of turpentine (see Terpenoids), and certain essential oils (see Oils, essential). A detailed calculation of steam distiUation of turpentine has been reported (85). [Pg.174]

Correlations for Enthalpy of Vaporization. Enthalpy or heat of vaporization, which is an important engineering parameter for Hquids, can be predicted by a variety of methods which focus on either prediction of the heat of vaporization at the normal boiling point, or estimation of the heat of vaporization at any temperature from a known value at a reference temperature (5). [Pg.234]

Example 2 Estimate the Critical Temperature and Critical Pressure of 2-Butanol, Which Has an Experimental Normal Boiling Point... [Pg.49]

Basic pure component constants required to characterize components or mixtures for calculation of other properties include the melting point, normal boiling point, critical temperature, critical pressure, critical volume, critical compressibihty factor, acentric factor, and several other characterization properties. This section details for each propeidy the method of calculation for an accurate technique of prediction for each category of compound, and it references other accurate techniques for which space is not available for inclusion. [Pg.384]

Equation (2-2), another somewhat simpler method for estimating the critical temperature of pure hydrocarbons only, is the method of Nokay " and requires the normal boiling point, the relative density, and the compound family. [Pg.384]

Equation (2-3) is the Lydersen equation for critical temperature and requires only the normal boiling point and the molecular structure for solution. [Pg.384]

Example 1 Estimate the critical temperature and critical pressure of 2-butanol using the Ambrose method, Eqs. (2-1) and (2-6). The experimental normal boiling point is 372.7 K. [Pg.386]

Various methods are available for estimation of the normal boiling point of organic compounds. Lyman et al. review and give calcula-tional procedures for the methods of Meissner, Miller, and Lydersen/ Forman-Thodos. A more recent method that has been determined to be more accurate is the method of Pailhes, which reqmres one experimental vapor pressure point and Lydersen group contributions for critical temperature and critical pressure (Table 2-385). [Pg.389]

Critical properties, if not available, can be estimated from tbe methods of tbe previous section. T,. is tbe reduced temperature at tbe temperature of interest, while Tr is tbe reduced temperature at tbe normal boiling point. [Pg.391]

The regression constants A, B, and D are determined from the nonlinear regression of available data, while C is usually taken as the critical temperature. The hquid density decreases approximately linearly from the triple point to the normal boiling point and then nonhnearly to the critical density (the reciprocal of the critical volume). A few compounds such as water cannot be fit with this equation over the entire range of temperature. Liquid density data to be regressed should be at atmospheric pressure up to the normal boihng point, above which saturated liquid data should be used. Constants for 1500 compounds are given in the DIPPR compilation. [Pg.399]

The method should not be used for the first member of a homologous series or for temperatures much above the normal boiling point (T 0.75). Errors for both hydrocarbons and nonhydrocarbons average 15 percent for a wide variety of compounds. Higher errors are noted for amines, diols, ethers, and fluorides. Table 2-398 gives AN and AB contributions for most common groups. Space prohibits examples for... [Pg.410]

Component 1 is the solute, while component 2 is water. The molar volume of the solute in mVkmole is at the solute normal boiling point, while the viscosity of water in Pa sec is at the temperature of the system resulting in a diffusivity in mVsec. The average error is about 9 percent when tested on 36 experimental systems. [Pg.416]

The boiling point of a liquid varies with the atmospheric pressure to which it is exposed. A liquid boils when its vapour pressure is the same as the external pressure on its surface, its normal boiling point being the temperature at which its vapour pressure is equal to that of a standard atmosphere (760mm Hg). Lowering the external pressure lowers the boiling point. For most substances, boiling point and vapour pressure are related by an equation of the form. [Pg.8]


See other pages where Temperature normal boiling point is mentioned: [Pg.942]    [Pg.1025]    [Pg.729]    [Pg.142]    [Pg.942]    [Pg.1025]    [Pg.729]    [Pg.142]    [Pg.88]    [Pg.7]    [Pg.7]    [Pg.165]    [Pg.440]    [Pg.504]    [Pg.504]    [Pg.38]    [Pg.259]    [Pg.37]    [Pg.234]    [Pg.234]    [Pg.253]    [Pg.212]    [Pg.319]   
See also in sourсe #XX -- [ Pg.23 , Pg.77 ]




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Temperature normal boiling

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