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Density values

Besides the expressions for a surface derived from the van der Waals surface (see also the CPK model in Section 2.11.2.4), another model has been established to generate molecular surfaces. It is based on the molecular distribution of electronic density. The definition of a Limiting value of the electronic density, the so-called isovalue, results in a boundary layer (isoplane) [187]. Each point on this surface has an identical electronic density value. A typical standard value is about 0.002 au (atomic unit) to represent electronic density surfaces. [Pg.129]

Elame-spread and smoke-density values, and the less often reported fuel-contributed semiquantitive results of the ASTM E84 test and the limited oxygen index (LOI) laboratory test, are more often used to compare fire performance of ceUular plastics. AH building codes requite that ceUular plastics be protected by inner or outer sheathings or be housed in systems aH with a specified minimum total fire resistance. Absolute incombustibHity cannot be attained in practice and often is not requited. The system approach to protecting the more combustible materials affords adequate safety in the buildings by aHowing the occupant sufficient time to evacuate before combustion of the protected ceUular plastic. [Pg.336]

Typical textile fibers used, for example, in a needle-punched filter fabric, are a blend of 3.3- and 6.6-dtex (3- and 6-denier) polyester staple. These fibers are - 5 cm long, have diameters ranging from 18 to 25 pm, mass-per-unit-length or linear density values ranging from - 350 to 650 mg per 1000 m, and length-to-width ratios in the order of 1000 to 1. [Pg.147]

The Flory-Huggins Interaction Parameter. These ideas, based on a study of polymer miscibility, have been appHed to plasticizers according to the foUowiag equation ia which is the molar volume of the plasticizer, obtaiaed from molar mass figures and density values at T, and represents the iateraction parameter (11). [Pg.124]

Compressibility. The bulk density of a soHd is an essential value used in the analysis of its flow properties, such as when calculating mass flow hopper angles, opening sizes, bin loads, etc. Loose and/or packed density values ate not sufficient. Bulk soHds exhibit a range of densities that vary as a function of consoHdating pressure. This range of densities, called the compressibiHty of the soHd, can often be expressed on a log—log plot as a line or relationship. [Pg.554]

A study on the thermodynamic properties of the three SO phases is given in Reference 30. Table 1 presents a summary of the thermodynamic properties of pure sulfur trioxide. A signiftcandy lower value has been reported for the heat of fusion of y-SO, 24.05 kj /kg (5.75 kcal/kg) (41) than that in Table 1, as have slightly different critical temperature, pressure, and density values (32). [Pg.175]

Charge density values calculated by Castle for all the pyridopyridazine parent systems are tabulated in (73HC(27)968 p. 989). [Pg.237]

Polarization and dipole moment studies for alkyl-, aryl-, carbonyl- hydroxy- (keto-) and amino-isoxazoles have been compiled and likewise support the low electron nature of the ring 63AHC(2)365, 62HC(l7)l,p. 177). More recent studies predict the order of electrophilic substitution to be 5>4> 3 on frontier electron density values of 0.7831, 0.3721 and 0.0659, respectively 7lPMH(4)237,pp.245,247). This contrasts with earlier reports of 4>5>3 on density values of —0.09, -t-0.14 and -t-0.18 in that order 63AHC(2 365). [Pg.4]

From Water Density at Atmospheric Pressure and Temperatures from 0 to 100°C, Tables of Standard Handbook Data, Standartov, Moscow, 1978. To conserve space, only a few tables of density values are given. The reader is reminded that density values may he found as the reciprocal of the specific volume values tabulated in the Thermodynamic Properties Tables subsection. [Pg.135]

From International Critical Tables, vol. 3, pp. 115-129. All compositions are in weight percent in vacuo. AU density values are dl = g/mL in vacuo. [Pg.153]

The density of a vapour or gas at eonstant pressure is proportional to its relative moleeular mass and inversely proportional to temperature. Sinee most gases and vapours have relative moleeular masses greater than air (exeeptions inelude hydrogen, methane and ammonia), the vapours slump and spread or aeeumulate at low levels. The greater the vapour density, the greater the tendeney for this to oeeur. Gases or vapours whieh are less dense than air ean, however, spread at low level when eold (e.g. release of ammonia refrigerant). Table 6.1 ineludes vapour density values. [Pg.180]

If the mesh is made of nickel, monel or copper, multiply the density values by 1.13, referenced to stainless steel. [Pg.248]

For density values g > 0.92 g/cm3 the deformation modes of the crystals predominate. The hard elements are the lamellae. The mechanical properties are primarily determined by the large anisotropy of molecular forces. The mosaic structure of blocks introduces a specific weakness element which permits chain slip to proceed faster at the block boundaries than inside the blocks. The weakest element of the solid is the surface layer between adjacent lamellae, containing chain folds, free chain ends, tie molecules, etc. [Pg.127]

The cross-section of 7-changing collisions found in Eq. (3.44) is sufficient for conversion of any gas density value to the quantity... [Pg.108]

Most vegetation maps are derived from a variety of sources using different methods and made at different times. This can lead to an overlap between adjacent areas of interest, the exclusion of some areas, and the improper extrapolation of carbon densities, thus resulting in inaccurate estimates of reservoir size. We found that the biomass density of the southern North American boreal forest was over 2.5 times larger than the biomass density of the northern part of the boreal forest (55). Past estimates of boreal forest biomass density extrapolated southern biomass density values to the entire boreal forest, which in part accounts for the large overestimation (7). It is important that a consistent method be developed to map vegetation globally. [Pg.421]

Monomer and Polymer Densities. Liquid density values at the relevant taiperature have been used (L5) a constant value for the polymer density, Pp, is assumed, indepandent of polymer c qposltlon and correspondent to the average of the homopalymer density values. [Pg.389]

When 2M methanol solution is fed to the stack at a flow rate of 2 ml/min and the stack is operated at a constant voltage output of 3.8V, the transient response of the stack current density is shown in Fig. 3 varying the flow rate of air to the cathode. The stack was maintained at a temperature of 50°C throughout the experiment. As shown in the figure, while the stack current is maintained at the air flow rates higher than 2 L/min, the stack current begins unstable at the slower flow rates. A similar result is shown in Fig. 4 for varying methanol flow rate at an air flow rate of 2 lymin. At a methanol flow rate of 8 ml/min, the current density reaches initially a current density value of about 130 mA/cm and then starts to decrease probably due to medianol crossover. As the methanol flow rate decreases, the stack current density increases slowly until the methanol flow rate reaches 3 ml/min because of the reduced methanol crossover. The current density drops rapidly from the methanol flow rate of 2 ml/min. [Pg.595]

For the computation of compressible flow, the pressure-velocity coupling schemes previously described can be extended to pressure-velocity-density coupling schemes. Again, a solution of the linearized, compressible momentum equation obtained with the pressure and density values taken from a previous solver iteration in general does not satisfy the mass balance equation. In order to balance the mass fluxes into each volume element, a pressure, density and velocity correction on top of the old values is computed. Typically, the detailed algorithms for performing this task rely on the same approximations such as the SIMPLE or SIMPLEC schemes outlined in the previous paragraph. [Pg.160]

TABLE 1. Receptor density values obtained from autoradiograms labeled with 3H-PCP, 3H-TCP and 3H-(+)SKh -t0,047 in rat brain... [Pg.30]


See other pages where Density values is mentioned: [Pg.555]    [Pg.2720]    [Pg.379]    [Pg.224]    [Pg.230]    [Pg.4]    [Pg.306]    [Pg.476]    [Pg.324]    [Pg.65]    [Pg.551]    [Pg.18]    [Pg.221]    [Pg.277]    [Pg.1913]    [Pg.127]    [Pg.23]    [Pg.440]    [Pg.16]    [Pg.87]    [Pg.554]    [Pg.419]    [Pg.420]    [Pg.62]    [Pg.108]    [Pg.220]    [Pg.151]    [Pg.152]    [Pg.376]   
See also in sourсe #XX -- [ Pg.610 , Pg.611 , Pg.612 ]

See also in sourсe #XX -- [ Pg.47 ]

See also in sourсe #XX -- [ Pg.138 ]

See also in sourсe #XX -- [ Pg.164 ]




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