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For volume

In an irreversible process the temperature and pressure of the system (and other properties such as the chemical potentials to be defined later) are not necessarily definable at some intemiediate time between the equilibrium initial state and the equilibrium final state they may vary greatly from one point to another. One can usually define T and p for each small volume element. (These volume elements must not be too small e.g. for gases, it is impossible to define T, p, S, etc for volume elements smaller than the cube of the mean free... [Pg.340]

Finally, for volumes of NaOH greater than the equivalence point volume, the pH is determined by the concentration of excess OH-. For example, after adding 30.0 mb of titrant the concentration of OH- is... [Pg.280]

Before the equivalence point, and for volumes of titrant in the titration curve s buffer region, the concentrations of HA and A are given by the following equations. [Pg.293]

For volumes of titrant before the equivalence point, a plot of Vb X [H3O+] versus Vb is a straight line with an x-intercept equal to the volume of titrant at the end point and a slope equal to Results for the data in Table 9.5 are shown in Table 9.6 and plotted in Figure 9.13d. Plots such as this, which convert a portion of a titration curve into a straight line, are called Gran plots. [Pg.293]

Equations 175 through 179 allow calculation of thermodynamic properties from volume-expHcit equations of state, ie, equations expHcitiy solvable for volume. If an equation of state is solvable expHcitiy for pressure but not for volume, then alternative formulas must be used, where p is molar density and subscript p/n = 1/E indicates constancy of total volume. Eor equations 180, 181, and 183, T and x are constant for equation 182, Tis constant. [Pg.496]

The hot mixes are designed by using a standard laboratory compaction procedure to develop a composition reflecting estabUshed criteria for volume percent air voids, total volume percent voids between aggregate particles, flow and stabdity, or compressive strength. Tests such as the Marshall, Unconfined Compression, Hubbard-Field, Triaxial Procedure, or the Hveem stabdometer method are used (109). [Pg.372]

Theorems of Pappus (for volumes and areas of surfaces of revolution)... [Pg.430]

Alternative Property Formulations Direct application of Eqs. (4-159) and (4-161) can be made only to equations of state that are solvable for volume, that is, that are volume explicit. Most equations of state are in fact pre.s.sure explicit, and alternative equations are required. [Pg.526]

TABLE 5-7 Mean Beam Lengths for Volume Radiation... [Pg.579]

Thermal expan sion of petroleum fuels can be estimated as volume change per unit volume per degree. ASTM-IP Petroleum Measurement Tables (ASTM D 1250 IP 200) are used for volume corrections in commercial transactions. [Pg.2364]

It can be seen drat the major difference lies in die activation energy being lower in the grain boundary. Data for a number of metals show that the activation energy for grain boundary diffusion is about one-half of that for volume diffusion. [Pg.198]

ADvFK for volume diffusion within die neck = 2DvFK for volume diffusion... [Pg.206]

He studied the sintering of copper particles in the diameter range 15-100 microns and of silver particles of diameter 350 microns. The results for the larger volume fraction of copper and for silver were shown to fit the volume diffusion mechanism and yielded the results for volume self-diffusion... [Pg.206]

Ashby pointed out diat die sintering studies of copper particles of radius 3-15 microns showed clearly the effects of surface diffusion, and die activation energy for surface diffusion is close to the activation energy for volume diffusion, and hence it is not necessarily the volume diffusion process which predominates as a sintering mechanism at temperatures less than 800°C. [Pg.207]

The apparent volume resistivity is dependent on the polarisation time (Figure 15.10). The initial polarisation current is effective for some time and if only a short time is allowed before taking measurements low values for volume resistivity will be obtained. [Pg.409]

Calibrate the detector tube pump for proper volume measurement at least quarterly. Simply connect the pump directly to the bubble meter with a detector mbe in-line. Use a detector mbe and pump from the same manufacturer. Wet the inside of the 100 cc bubble meter with soap solution. For volume calibration, experiment to get the soap bubble even with the zero ml mark of the buret. For piston-type pumps, pull the pump handle all the way out (full pump stroke) and note where the soap bubble stops for bellows-type pumps, compress the bellows fully for automatic pumps, program the pump to take a full pump stroke. [Pg.249]

The fourth source type option in SCREEN is for volume sources, which is selected by entering V or V for source type. The volume source algorithm is based on a virtual point source approach, and may be used for non-buoy ant sources whose emissions occupy some initial volume. The inputs requested for volume sources are as follows ... [Pg.312]

Table 3. Procedures for Estimating Initial Lateral Dimensions (Oyo) and Initial Vertical Dimensions (o ) for Volume Sources. Table 3. Procedures for Estimating Initial Lateral Dimensions (Oyo) and Initial Vertical Dimensions (o ) for Volume Sources.
Recently, the regulation of impeller rotational velocity has become a popular regulation mode for volume flow. Electric-motor rotational velocity is regulated by a frequency changer, and its price has dropped lately. Changing the rotational speed also affects the circumference velocity of the impeller. The volume flow can be changed by the same ratio as rotational speed. The form of the velocity triangles and the efficiency remain the same. [Pg.772]

Although the properties of specific polymer/wall systems are no longer accessible, the various phase transitions of polymers in confined geometries can be treated (Fig. 1). For semi-infinite systems two distinct phase transitions occur for volume fraction 0 = 0 and chain length N oo, namely collapse in the bulk (at the theta-temperature 6 [26,27]) and adsorp-... [Pg.557]

Unfortunately, some authors use the same symbol p for a number density and for volume charge distributions the electron density is (—e) times the number density.) The number density is a constant in this simple model. [Pg.213]


See other pages where For volume is mentioned: [Pg.59]    [Pg.311]    [Pg.320]    [Pg.87]    [Pg.250]    [Pg.344]    [Pg.58]    [Pg.654]    [Pg.1959]    [Pg.2237]    [Pg.2317]    [Pg.199]    [Pg.200]    [Pg.206]    [Pg.206]    [Pg.207]    [Pg.208]    [Pg.234]    [Pg.252]    [Pg.255]    [Pg.331]    [Pg.191]    [Pg.89]    [Pg.371]    [Pg.133]    [Pg.177]    [Pg.1432]   
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A realizable finite-volume scheme for bivariate velocity moments

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Additions and Corrections for Preceding Volumes

Author Index for Volumes

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Conservation Laws for Control Volumes

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Contents for Volumes

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Elements of the Finite Volume Method for Flow Simulations

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Energy Balances for Volume Zones—The Radiation Source Term

Engineering for the Treatment of Gases, Volume

Errata for Volume

Explicit Expression for the Excess Volume

Extensions of Polanyis theory for micropore volume and area

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Finite Volume Method for Calculation of Flow Field

Finite Volume Methods for Multi-fluid Models

Finite volume method for

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Injection volume for

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List of Contributors for Volumes

Maximum Sample Injection Volume for a Specific Column

Models for Prediction of Volume

Models for the standard partial molar volume

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Part I Adsorption Methods for Determination of Surface Areas and Pore Volumes

Perturbation calculation for the excluded volume effect

Phial filler for large volumes

Pressure-Volume-Temperature Relationship for Polymer Melts

Pressure-Volume-Temperature Relationships for Polymer

Proof that volume mol (for ideal gases)

Rate equations for constant-volume batch reactors

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Realizable finite-volume schemes for moments

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Sample Plates for Low-Volume High-Throughput Screening

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Series for previous volumes

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Standard finite-volume schemes for moments

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