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Flow mixing systems

Appendix 2 is an example of the way in which the transfer function of a flow-mixing system may be used to predict the conversion of reactant which will be achieved in that system when a reaction with first-order kinetics is occurring. This short-cut route is used extensively later in this chapter. [Pg.224]

It is clear that, in the particular case illustrated, all material has a residence time of between to and t2 minutes and therefore the mean or average time spent in the system is between these two extremes. For a flow-mixing system in which no adsorption, reaction or change in volume flow rate occurs, this mean residence time is always equal to the volumetric holdup of the system divided by the constant flow rate through the system [1]. Thus, the mean residence time, t, equals V/Q and is seen to be identical... [Pg.225]

The most general form of the recycle flow mixing system is illustrated in Fig. 13. [Pg.257]

For simplicity, in this section we have again largely restricted our attention to first-order reactions. General design charts of the form of Fig. 14 can, in principle, be constructed for any recycle flow-mixing system and any form of kinetics. [Pg.260]

It might be expected that all recycle flow-mixing systems would give a performance the same as that of an equal size CSTR for infinitely large recycle ratios. This is not necessarily so and, recently, considerable attention has been focused on various forms of Gj (s) and G2(s), in Fig. 13, which exhibit surprising behaviour in this respect. References 50—54 are concerned with this problem. [Pg.260]

Some comments on estimating parameters in flow-mixing systems... [Pg.267]

The advantages of the bipolar pulse technique include speed (discrete measurements at a rate as high as 30 kHz), accuracy, and signal-to-noise ratio. The system has been employed as a detector in automated conductometric titrations and in stopped-flow mixing systems with excellent results. [Pg.262]

The design of the instrument will be discussed primarily on the block diagram level. Details on the construction of the vidicon spectrophotometer (19), the multi-microcomputer system (20) and the stopped-flow mixing system (20) are presented elsewhere. [Pg.170]

Clusters, continuous flow mixing systems, 93ff... [Pg.188]

Fig. 21. Generalized scheme of flow-mix system, showing mixing chamber M and observation... Fig. 21. Generalized scheme of flow-mix system, showing mixing chamber M and observation...
Some of the minor accessories used in ESR spectroscopy, which can be viewed logically as separate instrumental sub-systems, are (10) temperature control systems (11) photoexcitation systems (12) electrochemical systems (13) continuous and stopped flow mixing systems. [Pg.129]

Fit . 4. EPR spectrum observed immediately after mixing soybean Fe(III) Lb (250 fj.M) with HA (250 p,M) at pH 7.4. Reaction studied using a two-way stopped-flow mixing system inserted into the cavity of the EPR spectrometer. The signal is assigned to a sterically constrained tyrosine phenoxyl radical formed at position 133 (reproduced with permission from Davies, M. J. Puppo, A. Biochem. J. 1992, 281, 197—201). [Pg.513]

For many readers, the term "construction principle may mean much more than a twinning the calorimeter can also be built liquid or aneroid, closed or open, in a Dewar, with a liquid thermostat or a furnace, with thermopiles or thermistors, with a batch or liquid flow mixing system, with a steady flame or a bomb combustion device, with a sample drop facility and with a multi-sampler). [Pg.43]


See other pages where Flow mixing systems is mentioned: [Pg.115]    [Pg.267]    [Pg.93]    [Pg.189]    [Pg.190]    [Pg.115]    [Pg.397]    [Pg.115]    [Pg.21]   
See also in sourсe #XX -- [ Pg.249 , Pg.267 ]




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