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Mixing, time

Now let us consider the mixing time, t. This will be estimated by an order of magnitude estimate for diffusion to occur across the boundary layer thickness, 5Bl- If we have turbulent natural conditions, it is common to represent the heat transfer in terms of the Nusselt number for a vertical plate of height, , as [Pg.162]

we see that this mixing time is also very small. However, this analysis implicity assumed that the pilot is located where the fuel vapor evolved. A pilot downstream would introduce an additional transport time in the process. [Pg.163]

The variation of measured mixing time with gas fiow rate for three different vessels are presented in Figs. 5.38,5.39 and 5.40. The straight line in each figure represents the best fit of the measured data for the same aspect ratio. The mixing time decreases with an increase in the gas flow rate, but increases with an increase in the bath diameter. The following empirical relation has been proposed for the mixing time in a bottom blown bath in the absence of swirl motion [52], [Pg.204]

In the above equations, g is the acceleration due to gravity and Re is the Reynolds number based on the superficial velocity of gas, E p. The conditions describing the onset of swirl motion have been given Sect. 5.2.3.1 [29,30]. [Pg.206]

Inspection of Fig. 5.41 suggests that the coefficient ak is a function of the vessel diameter D. [Pg.206]

Referring to Stokes s first problem [56], we introduce the following representative length to non-dimensionalize the vessel diameter as follows [Pg.206]

For convenience, k is assumed to be unity and (5.30) is substituted into (5.29) to give [Pg.207]


A proposal based on Onsager s theory was made by Landau and Lifshitz [27] for the fluctuations that should be added to the Navier-Stokes hydrodynamic equations. Fluctuating stress tensor and heat flux temis were postulated in analogy with the Onsager theory. Flowever, since this is a case where the variables are of mixed time reversal character, tlie derivation was not fiilly rigorous. This situation was remedied by tlie derivation by Fox and Ulilenbeck [13, H, 18] based on general stationary Gaussian-Markov processes [12]. The precise fomi of the Landau proposal is confimied by this approach [14]. [Pg.705]

The interval between the second and third pulse is called the mixing time, during which the spins evolve according to the multiple-spin version of equation B 1.13.2 and equation B 1.13.3 and the NOE builds up. The final pulse converts the longitudinal magnetizations, present at the end of the mixing time, into detectable transverse components. The detection of the FID is followed by a recycle delay, during which the equilibrium... [Pg.1510]

Figure Bl.13.7. Simulated NOESY peak intensities in a homoniielear two-spin system as a fiinetion of the mixing time for two different motional regimes. (Reprodiieed by pennission of Wiley from Neiihaiis D 1996 Encyclopedia of Nuclear Magnetic Resonance ed D M Grant and R K Harris (Chiehester Wiley) pp 3290-301.)... Figure Bl.13.7. Simulated NOESY peak intensities in a homoniielear two-spin system as a fiinetion of the mixing time for two different motional regimes. (Reprodiieed by pennission of Wiley from Neiihaiis D 1996 Encyclopedia of Nuclear Magnetic Resonance ed D M Grant and R K Harris (Chiehester Wiley) pp 3290-301.)...
The time resolution of these methods is detennined by the time it takes to mitiate the reaction, for example the mixing time in flow tubes or the laser pulse width in flash photolysis, and by the time resolution of the detection. Relatively... [Pg.2116]

Single-base propellants are mixed in a similar fashion by adding the ingredients to the nitrocellulose in the mixer together with the required amounts of ether and alcohol. The mixing time is about one-half hour, and the temperature is kept below 25°C. The pardy colloidal mixture looks like moist cmde sugar. A maceration step may be included to increase homogeneity. [Pg.44]

Bakery Products. Sorbates are used in and/or on yeast-raised and chemically leavened bakery products. The internal use of sorbates in yeast-raised products at one-fourth the amount of calcium—sodium propionate that is normally added provides a shelf life equal to that of propionate without adversely affecting the yeast fermentation. Sorbates added at one-tenth the propionate level reduce the mix time by 30% (126). This internal treatment combined with an external spray of potassium sorbate can provide the same or an increased shelf life of pan breads, hamburger and hot-dog buns, English muffins, brown-and-serve roUs, and tortillas. The total sorbate useful in or on these baked goods ranges from 0.03 wt % for pan breads to 0.5 wt % for tortillas 0.2—0.3 wt % sorbic acid protects chemically leavened yellow and chocolate cakes (127). Emit-pie fillings and icings can be protected with 0.03—0.1 wt % sorbates. [Pg.287]

SBR mbber compounds are prepared in two stages the nonproductive and the productive phases. In the nonproductive phase the compound ingredients are mixed, usually in internal mixers (Banbury). The mixing time is usually short and the compound temperature is in the 160—195°C range. [Pg.499]

Not only is the type of flow related to the impeller Reynolds number, but also such process performance characteristics as mixing time, impeller pumping rate, impeller power consumption, and heat- and mass-transfer coefficients can be correlated with this dimensionless group. [Pg.1629]

Likewise, large-diameter impellers (D > Df/2) are useful for (1) avoiding stagnant regions in slurries, (2) short mixing times to obtain uniformity throughout a vessel, (3) promotion of heat transfer, and (4) laminar continuous averaging of slurries. [Pg.1630]

Propeller size, pitch, and rotational speed may be selected by model tests, by experience with similar operations, or, in a few cases, by published correlations of performance data such as mixing time or heat transfer. The propeller diameter and motor power should be the minimum which meet process requirements. [Pg.1631]

A double helix shortens mixing time but requires more power. The disadvantages of the higher torque requirement are freqiientlv offset bv the better mixing and heat transfer,... [Pg.1644]

Care should be taken to avoid mixing too long, as in some cases this will result in a poorer blend. A graph of degree of mixing versus time should be made to selecl the proper mixing time quantitatively. [Pg.1766]


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Agglomerates, mixing time

Agitation mixing time

Assumption of ideal mixing. Residence time

Axial Mixing and Residence Time Distribution

Backmixing residence time distribution and micro-mixing

Bead-blood mixing time

Bioreactors liquid mixing time

Bromine mixing time with

Characteristic mixing time analysis

Circulation and mixing times in turbulent agitated tanks

Compounding mixing time

Dead time after mixing reactants

Dead time stopped-flow mixing

Deep mixing time

Dispersion models, mixing residence-time distribution

Distribution function reaction time, mixing

Dough optimum mixing time

Effect of the mixing time

Errors mixing, retention times

Experimental Methods for Determining Mixing Quality and Residence Time Distribution

Flour mixing time

Flow time-pulsing mixing

Four-wave mixing time delayed

H COSY with Varying Mixing Times for the Coupling

HOESY mixing time

Hydrogen mixing time with

Induction time mixing

Macroscopic mixing time

Mechanically liquid mixing time

Micro-channels mixing time

Mixed time-frequency representation

Mixing Time ENDOR

Mixing Times and Scaleup

Mixing circulation time, shear rates

Mixing in Residence Time Space

Mixing or Residence Time

Mixing residence time

Mixing residence time distribution

Mixing residence time space

Mixing time analysis

Mixing time characteristics

Mixing time characteristics -♦ Homogenization

Mixing time correction, stopped-flow

Mixing time correlation

Mixing time, electrophoretically

Mixing time, global

Mixing time, measurement

Mixing-time dependence

Multi mixing time

NMR spectroscopy mixing time

NOESY zero mixing time

Note on Times of Mixing in the Atmosphere and Oceans

Of mixing times

Plug flow, mixing model residence-time distribution

Powder mix time

Quantitative Measurement of the Mixing Time

ROESY mixing time

Rate and time for mixing

Rate and time of mixing

Reaction and Mixing Times

Reaction time distribution mixing theory

Residence Time Distribution A Tool for Analysis of Fluid Mixing Pattern

Residence time distribution function perfectly mixed reactors

Residence time mixing chamber

Setting times mixing and placing

Simulation time-pulsing mixing

Stirred Vessels Liquid Mixing Time

Stirring and mixing time

Time Scales of Mixing in the Atmosphere and Oceans

Time scale mixing, reaction

Time scale turbulent mixing

Time scale, micro-mixing

Time scales mixing

Time-Dependent Turbulent Mixing and Chemical Reaction in Stirred Tanks

Time-delayed four-wave mixing with

Time-dependent mixed quantum classical

Time-dependent mixed quantum classical approaches

Time-pulsing mixing

Troposphere mixing times

Turbulent mixing blend time

Variable mixing time

Wheat dough mixing time

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