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Molar diagram

Molar diagram A plot of the thermodynamic properties of a substance that has specific enthalpy as one of its coordinates. [Pg.1460]

Few if any binary mixtures are exactly syimnetrical around v = 1/2, and phase diagrams like that sketched in figure A2.5.5(c) are typicd. In particular one can write for mixtures of molecules of different size (different molar volumes and F°g) the approxunate equation... [Pg.629]

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]

Fig. 4.24 Heat of immersion of a carbon (prepared by pyrolysis of Saran Polymer A) in different liquids at 300 K. The liquids for points 1-6 were (I) methanol (2) benzene (3) n-hexane (4) 3-methyl benzene (5) 2,2-dimethyl butane (6) 2,2,4-trimethyl pentane. The abscissae represent the molar volumes of the liquids. (Redrawn from the original diagram of Barton, Beswick and Harrison. " )... Fig. 4.24 Heat of immersion of a carbon (prepared by pyrolysis of Saran Polymer A) in different liquids at 300 K. The liquids for points 1-6 were (I) methanol (2) benzene (3) n-hexane (4) 3-methyl benzene (5) 2,2-dimethyl butane (6) 2,2,4-trimethyl pentane. The abscissae represent the molar volumes of the liquids. (Redrawn from the original diagram of Barton, Beswick and Harrison. " )...
Fig. 5.2 Type III isotherms, (a) n-hexane on PTFE at 25°C (b) n-octane on PTFE at 20 C (c) water on polymethylmethacrylate at 20°C (d) water on bis(A-polycarbonate) (Lexan) at 20°C. The insets in (c) and (d) give the curves of heat of adsorption against fractional coverage the horizontal line marks the molar heat of liquefaction. (Redrawn from diagrams in the original papers, with omission of experimental points.)... Fig. 5.2 Type III isotherms, (a) n-hexane on PTFE at 25°C (b) n-octane on PTFE at 20 C (c) water on polymethylmethacrylate at 20°C (d) water on bis(A-polycarbonate) (Lexan) at 20°C. The insets in (c) and (d) give the curves of heat of adsorption against fractional coverage the horizontal line marks the molar heat of liquefaction. (Redrawn from diagrams in the original papers, with omission of experimental points.)...
The freezing point diagram for the hydrazine—water system (Eig. 1) shows two low melting eutectics and a compound at 64 wt % hydrazine having a melting point of —51.6°C. The latter corresponds to hydrazine hydrate [7803-57-8] which has a 1 1 molar ratio of hydrazine to water. The anomalous behavior of certain physical properties such as viscosity and density at the hydrate composition indicates that the hydrate exists both in the Hquid as well as in the soHd phase. In the vapor phase, hydrazine hydrate partially dissociates. [Pg.273]

Figure 3 is the humidity chart diagram in molar quantities where enthalpy deviations are not given. Enthalpy may also be calculated from the enthalpy of saturated air and of dry air using % saturation ... [Pg.98]

Operating Lines The McCabe-Thiele method is based upon representation of the material-balance equations as operating lines on the y-x diagram. The lines are made straight (and the need for the energy balance obviated) by the assumption of constant molar overflow. The liqmd-phase flow rate is assumed to be constant from tray to tray in each sec tiou of the column between addition (feed) and withdrawal (produc t) points. If the liquid rate is constant, the vapor rate must also be constant. [Pg.1265]

With these facts in mind, it seems reasonable to calculate the pore volume from the calibration curve that is accessible for a certain molar mass interval of the calibration polymer. A diagram of these differences in elution volume for constant M or AM intervals looks like a pore size distribution, but it is not [see the excellent review of Hagel et al. (5)]. Absolute measurements of pore volume (e.g., by mercury porosimetry) show that there is a difference on principle. Contrary to the absolute pore size distribution, the distribution calcu-... [Pg.437]

After filling the receiver, reflux runs down the column at the same molar rate as the vapor back up (L = G). The operating line has a slope of 1.0. Then there are n plates/trays between composition Xp and xj (the mol fraction in distillate). As the distillation continues, the operating line moves closer to the 45° line of the diagram, and x and Xp (and Xj) become richer and leaner, respectively, until at the end xj becomes Xq and x becomes x. The required time is 02. [Pg.47]

Vmin = Minimum fresh air flow based on slope of operating line, L/V, on x-y diagram V = Vapor flowrate, mols/hr or molar volume W = Bottoms product, or still bottoms, or ketde bottoms, mols also see B or mols/hr bottoms product or mols of residue or bottoms/unit time (Ponchon heat balance)... [Pg.106]

In order to draw the property - composition diagram, coordinates are usually chosen so that the ideal system values correspond with the additive law regarding concentration [313]. It is known, for instance, that in an ideal system, molar volume changes additively with the concentration, and is expressed in molar fractions or molar percentages, whereas specific volume changes linearly with the concentration, and is expressed in mass fractions or mass percentages. [Pg.148]

Fig. 3. Schematic diagram for the variation with concentration of the partial molar heat of solution of the liquid noble metals into liquid tin, taken from reference 51. The numbers are the experimental and calculated AHt for the solutes, in cal/g atom, at the two concentrations of 0 and 0.02 mole fraction. Q-C labels the curves calculated by the quasichemical theory in first order B-W labels the curves calculated by the Bragg-Williams, or zeroth-order approximation, which assumes a random... Fig. 3. Schematic diagram for the variation with concentration of the partial molar heat of solution of the liquid noble metals into liquid tin, taken from reference 51. The numbers are the experimental and calculated AHt for the solutes, in cal/g atom, at the two concentrations of 0 and 0.02 mole fraction. Q-C labels the curves calculated by the quasichemical theory in first order B-W labels the curves calculated by the Bragg-Williams, or zeroth-order approximation, which assumes a random...
The production rate of acetic acid was 2kg-h 1, where the maximum acetic acid concentration was 12%. Air was pumped into the fermenter with a molar flow rate of 200 moMi-. The chemical reaction is presented in (E. 1.1) and flow diagram in Figure 9.5. Determine the minimum amount of ethanol intake and identify the required mass balance for the given flow sheet. The ethanol biochemical oxidation reaction using A. aceti is ... [Pg.239]

Figure 6.3 Diagram of apparatus for determining molar mass by light scattering... Figure 6.3 Diagram of apparatus for determining molar mass by light scattering...
Unlike low molar mass liquid crystals, these materials do not undergo a nematic-isotropic transition. Instead, they adopt liquid crystal behaviour throughout the region of the phase diagram for which they are in the melt. Above a particular temperature, rather than adopting an isotropic liquid structure, they decompose. [Pg.157]

Intermetallic compounds are generally prepared by simply heating the elements in the correct molar proportion at or just below the liquidus temperature specified in the phase diagram. The major experimental problems associated with these methods are first, attack of the container material by the alkali metal or the intermetallic compound in the molten state second, the temperature chosen must be such as to attain true homogeneity of the intermetallic compound. [Pg.413]

Fig. 4.2 Part of the phase diagram of the system praseodymium-iodine (Pr/I) the abscissa is drawn as molar fractions of Pr in Pr s. Reproduced from Ref [1]. Fig. 4.2 Part of the phase diagram of the system praseodymium-iodine (Pr/I) the abscissa is drawn as molar fractions of Pr in Pr s. Reproduced from Ref [1].
The model equations, I to V above, provide the basis for solution, for this case of constant temperature and pressure with a molar change owing to chemical reaction. This is illustrated by the information flow diagram. Fig. 4.10. The step-by-step calculation procedure is as follows ... [Pg.238]

Figure 4.10. Information flow diagram for a gas-phase tubular reactor with molar change. Figure 4.10. Information flow diagram for a gas-phase tubular reactor with molar change.
Fig. 31 Phase diagram of type III for PVME in water with two different molar masses hand-drawn curves). T em Mw = 28000 gmol-1 ( ) and Mw = 147000 gmol-1 (A). Peak temperature Tmax Mw = 28 000 g mol-1 ( ) and Mw = 147 000 g mol-1 (T). Cloud point for Mw = 147000gmol-1 ( ). Scanning rate 0.1 °Cmin-1. (Reprinted with permission from Ref. [161] copyright 1997 American Chemical Society)... Fig. 31 Phase diagram of type III for PVME in water with two different molar masses hand-drawn curves). T em Mw = 28000 gmol-1 ( ) and Mw = 147000 gmol-1 (A). Peak temperature Tmax Mw = 28 000 g mol-1 ( ) and Mw = 147 000 g mol-1 (T). Cloud point for Mw = 147000gmol-1 ( ). Scanning rate 0.1 °Cmin-1. (Reprinted with permission from Ref. [161] copyright 1997 American Chemical Society)...

See other pages where Molar diagram is mentioned: [Pg.649]    [Pg.483]    [Pg.187]    [Pg.175]    [Pg.47]    [Pg.460]    [Pg.239]    [Pg.190]    [Pg.392]    [Pg.458]    [Pg.23]    [Pg.398]    [Pg.383]    [Pg.34]    [Pg.392]    [Pg.397]    [Pg.413]    [Pg.156]    [Pg.56]    [Pg.24]    [Pg.26]    [Pg.27]    [Pg.30]    [Pg.31]    [Pg.47]    [Pg.73]   
See also in sourсe #XX -- [ Pg.1461 ]




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