Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Flow process maximum velocity

It has been suggested, however, that for mass transfer, the transfer in the liquid phase is from a vapour-liquid interface where the liquid velocity is a maximum to the wall where it is zero. With a liquid flowing inside the tube the heat transfer is from a layer of zero velocity at the wall to the fluid all the way to the centre of the tube where it is moving with a maximum velocity. Hatta 79-1 based his analysis on the more closely related process of diffusion of a gas into a liquid, and obtained the expression ... [Pg.648]

In order to analyze the atomization mechanism of the air-shrouded injector, the atomization characteristics of the fabricated atomizer was investigated using a phase Doppler particle analyzer (PDPA). The Sauter mean diameter (SMD) and mean velocity distribution at 5 ms ASI are shown in Fig. 34.8. As the air pressure increases, the air velocity increases and the air dispersion area is enlarged proportionally. The maximum velocity achieved is 55 m/s when the air pressure is 50 kPa. The degree of atomization is greater at the center flow because the air velocity at the center flow is greater. Spray patterns for various air pressures are shown in Fig. 34.9. It can be seen that as the air pressure increases, the atomization process transitions from varicose wave to sinuous wave mode. Atomization at low air pressure and low fuel pressure can be seen to be affected by a twisted or sinuous mode. The spray angle... [Pg.783]

The maximum velocity of flow that can be attained is the speed of sound. It is reached for the critical pressure ratio Wi ji, and true as well if w < Wknt- The flow rate then only depends on the pressure inside the enclosure, pi, and not on the external pressure, p2. Equation (7.20) hence applies for discharge processes with velocities below the speed of sound and Eq. (7.23) for all other cases. The latter is usually required if gas under high pressure is discharged. [Pg.241]

The experimental results of dynamic pressurization show, that this method is suitable for the determination not only the measturement of pressurization velocity, but the real adsorption velocity too. That will bridge over the difficulties originated from the differences among industrial appUcations and the equilibrium or very slow scientific measurements. With the help of these equipments the RPSA processes can be carefuUy examined. This system is new in this field in the sense of high fi quency as well as the easy data acquition. The maximum velocities of different mass flows show the boundary values of URPSA technologies (Table 1). [Pg.293]

Evolution of the fitness function and the design variables during the optimization process are respectively shown in Fig.6 and Fig.7. The optimized result of the flow velocity distribution on the outlet is shown in Fig.8. The velocity distribution both before and after optimization in the centerline of Y-Axis on the outlet cross-section is extracted and shown in Fig.9. Curve A is the velocity distribution after optimization and curve B is what before. Velocity distribution of Curve A is relatively uniform by comparison. The maximum velocity difference decreased by 46% which shows that the optimization approach presented in our study is feasible. [Pg.95]

The mean residence time T (defined as H JF) is the most important parameter, since it determines the time over which particles are exposed to grinding. Measurements on several industrial mills (Weller, Automation in Mining Mineral and Metal Processing, 3d IFAC Symposium, 303-309, 1980) (measured on the water, not the ore) showed that the maximum mill filhng was about 40 percent, and the maximum flow velocity through the mill is 40 m/h. [Pg.1851]

To improve the mixing quality in the tubular reactor, Kenics type in-line static mixer reactor was employed. The in-line static mixers were designed to mix two or more fluids efficiently since an improved treinsport process such as flow division, radial eddying, flow constriction, and shear reversal eliminated the gradients in concentration, velocity and temperature. However, only 70 % conversion was achieved with one Kenics mixer unit. As shown in Table 2, five mixer units were required to achieve the maximum conversion. [Pg.651]


See other pages where Flow process maximum velocity is mentioned: [Pg.83]    [Pg.120]    [Pg.119]    [Pg.1258]    [Pg.323]    [Pg.482]    [Pg.577]    [Pg.441]    [Pg.274]    [Pg.1673]    [Pg.1746]    [Pg.270]    [Pg.212]    [Pg.60]    [Pg.1669]    [Pg.1740]    [Pg.83]    [Pg.1439]    [Pg.533]    [Pg.57]    [Pg.324]    [Pg.391]    [Pg.141]    [Pg.415]    [Pg.48]    [Pg.54]    [Pg.65]    [Pg.64]    [Pg.435]    [Pg.177]    [Pg.38]    [Pg.293]    [Pg.117]    [Pg.109]    [Pg.1168]    [Pg.292]    [Pg.88]    [Pg.338]    [Pg.258]    [Pg.395]   
See also in sourсe #XX -- [ Pg.219 , Pg.220 , Pg.221 ]




SEARCH



Flow velocity

Maximum flow

Process flow

Process flow processing

© 2024 chempedia.info