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Residence function

In most of these studies, hydroxyl has been the typical resident functional group, which is derivatized with appropriate acids containing chromophores suitable for exciton coupling. The ideal chromophore would have a very intense UV-visible transition, located in a convenient spectral window, and with the orientation of its electric transition moment being well-defined relative to alcohol R—OH bond. One of the most successful has been p-dimethylaminobenzoate, which has an intense (s ca 30, 000) transition in an... [Pg.241]

Techniques for evaluating processing stabiHty and mechanochemical effects include using a Brabender torque rheometer (29,30), injection mol ding (26,28), capillary rheometry (26,28), and measuring melt index as a function of residence time (26). [Pg.203]

Flotation process kinetics determine the residence time, the average time a given particle stays in the flotation pulp from the instant it enters the ceU until it exits. One way to study flotation kinetics is to record flotation recoveries as a function of time under a given set of conditions such as pulp pH, coUector concentration, particle size, etc. The data allow the derivation of an expression that describes the rate of the process. [Pg.49]

An analytical model of the process has been developed to expedite process improvements and to aid in scaling the reactor to larger capacities. The theoretical results compare favorably with the experimental data, thereby lending vahdity to the appHcation of the model to predicting directions for process improvement. The model can predict temperature and compositional changes within the reactor as functions of time, power, coal feed, gas flows, and reaction kinetics. It therefore can be used to project optimum residence time, reactor si2e, power level, gas and soHd flow rates, and the nature, composition, and position of the reactor quench stream. [Pg.393]

The classical experiment tracks the off-gas composition as a function of temperature at fixed residence time and oxidant level. Treating feed disappearance as first order, the pre-exponential factor and activation energy, E, in the Arrhenius expression (eq. 35) can be obtained. These studies tend to confirm large activation energies typical of the bond mpture mechanism assumed earlier. However, an accelerating effect of the oxidant is also evident in some results, so that the thermal mpture mechanism probably overestimates the time requirement by as much as several orders of magnitude (39). Measurements at several levels of oxidant concentration are useful for determining how important it is to maintain spatial uniformity of oxidant concentration in the incinerator. [Pg.57]

Oxidation of cumene to cumene hydroperoxide is usually achieved in three to four oxidizers in series, where the fractional conversion is about the same for each reactor. Fresh cumene and recycled cumene are fed to the first reactor. Air is bubbled in at the bottom of the reactor and leaves at the top of each reactor. The oxidizers are operated at low to moderate pressure. Due to the exothermic nature of the oxidation reaction, heat is generated and must be removed by external cooling. A portion of cumene reacts to form dimethylbenzyl alcohol and acetophenone. Methanol is formed in the acetophenone reaction and is further oxidized to formaldehyde and formic acid. A small amount of water is also formed by the various reactions. The selectivity of the oxidation reaction is a function of oxidation conditions temperature, conversion level, residence time, and oxygen partial pressure. Typical commercial yield of cumene hydroperoxide is about 95 mol % in the oxidizers. The reaction effluent is stripped off unreacted cumene which is then recycled as feedstock. Spent air from the oxidizers is treated to recover 99.99% of the cumene and other volatile organic compounds. [Pg.288]

Flotation. Flotation (qv) is used alone or in combination with washing and cleaning to deink office paper and mixtures of old newsprint and old magazines (26). An effective flotation process must fulfill four functions. (/) The process must efficiently entrain air. Air bubble diameter is about 1000 p.m. Typically air bubbles occupy 25—60% of the flotation cell volume. Increa sing the airRquid ratio in the flotation cell is said to improve ink removal efficiency (27). (2) Ink must attach to air bubbles. This is primarily a function of surfactant chemistry. Air bubbles must have sufficient residence time in the cell for ink attachment to occur. (3) There must be minimal trapping of cellulose fibers in the froth layer. This depends on both cell design and surfactant chemistry. (4) The froth layer must be separated from the pulp slurry before too many air bubbles coUapse and return ink particles to the pulp slurry. [Pg.8]

A succession of federal agencies and adininistrations has been charged with dealing with wastewater. At present this responsibility resides with the EPA. It has been proposed that most of the EPA functions be turned back to the states. It remains to be seen if the states, with conflicting needs and priorities, will be able to deal successfully with these problems. [Pg.286]

Carbon Conversion. Carbon conversion on a once-through basis is a function of the coal composition and is strongly influenced by the oxygen/coal ratio. For some coals, the conversion pattern is also affected by the level of steam in the blast. Another factor is fly slag recycle, which raises the carbon conversion by recycling the unconverted carbon, most of which resides on the fly slag. This results in an overall carbon conversion greater than 99%. [Pg.274]

Fig. 10. (a) Rockwell flash hydiopyiolysis leactoi and (b) caibon conveision as a function of leactoi residence time. The reaction was mn at 1038°C and... [Pg.289]

As an idealization of the classified-fines removal operation, assume that two streams are withdrawn from the crystallizer, one corresponding to the product stream and the other a fines removal stream. Such an arrangement is shown schematically in Figure 14. The flow rate of the clear solution in the product stream is designated and the flow rate of the clear solution in the fines removal stream is set as (R — 1) - Furthermore, assume that the device used to separate fines from larger crystals functions so that only crystals below an arbitrary size are in the fines removal stream and that all crystals below size have an equal probabiHty of being removed in the fines removal stream. Under these conditions, the crystal size distribution is characterized by two mean residence times, one for the fines and the other for crystals larger than These quantities are related by the equations... [Pg.351]

The production rate is 2—4 t/h, depending on the feed rate, monomer concentration in the feed, and conversion. The conversion of isobutylene and isoprene typically ranges from 75—95% and 45—85%, respectively, depending on the grade of butyl mbber being produced. The composition and mol wt of the polymer formed depend on the concentration of the monomers in the reactor Hquid phase and the amount of chain transfer and terminating species present. The Hquid-phase composition is a function of the feed composition and the extent of monomer conversion. In practice, the principal operating variable is the flow rate of the initiator/coinitiator solution to the reactor residence time is normally 30—60 minutes. [Pg.482]

In turbulent flow, axial mixing is usually described in terms of turbulent diffusion or dispersion coefficients, from which cumulative residence time distribution functions can be computed. Davies (Turbulence Phenomena, Academic, New York, 1972, p. 93), gives Di = l.OlvRe for the longitudinal dispersion coefficient. Levenspiel (Chemical Reaction Engineering, 2d ed., Wiley, New York, 1972, pp. 253-278) discusses the relations among various residence time distribution functions, and the relation between dispersion coefficient and residence time distribution. [Pg.638]

Composition The law of mass aclion is expressed as a rate in terms of chemical compositions of the participants, so ultimately the variation of composition with time must be found. The composition is determined in terms of a property that is measured by some instrument and cahbrated in terms of composition. Among the measures that have been used are titration, pressure, refractive index, density, chromatography, spectrometry, polarimetry, conduclimetry, absorbance, and magnetic resonance. In some cases the composition may vary linearly with the observed property, but in every case a calibration is needed. Before kinetic analysis is undertaken, the data are converted to composition as a function of time (C, t), or to composition and temperature as functions of time (C, T, t). In a steady CSTR the rate is observed as a function of residence time. [Pg.707]

For the consecutive reactions 2A B and 2B C, concentrations were measured as functions of residence time in a CSTR. In all experiments, C o = 1 lb moPfF. Volumetric flow rate was constant. The data are tabulated in the first three columns. Check the proposed rate equations,... [Pg.710]

Irrespective of the protocol used, communication programs act as servers to the database manager. When some functions request data from a remote node, the database manager will transfer the request to the remote node database manager via the communication programs. The remote node communication programs will relay the request to the resident database manager and return the obtained data. The remote database access and the existence of communications equipment and software are transparent to plant operators. [Pg.775]

Digital Field Communications An increasing number of valve-mounted devices are available that support digital communications in addition to, or in place of, the traditional 4—20 mA current signal. These control-valve devices have increased functionality, resulting in reduced setup time, improved control, combined functionality of traditionally separate devices, and control-valve diagnostic capabihty. Digital communications also allow the control system to become completely distributed where, for example, the process PID controller could reside in the valve positioner or in the process transmitter. [Pg.786]


See other pages where Residence function is mentioned: [Pg.204]    [Pg.164]    [Pg.61]    [Pg.648]    [Pg.56]    [Pg.296]    [Pg.346]    [Pg.387]    [Pg.76]    [Pg.204]    [Pg.164]    [Pg.61]    [Pg.648]    [Pg.56]    [Pg.296]    [Pg.346]    [Pg.387]    [Pg.76]    [Pg.100]    [Pg.650]    [Pg.200]    [Pg.254]    [Pg.203]    [Pg.345]    [Pg.156]    [Pg.35]    [Pg.354]    [Pg.449]    [Pg.172]    [Pg.233]    [Pg.415]    [Pg.554]    [Pg.125]    [Pg.510]    [Pg.413]    [Pg.294]    [Pg.211]    [Pg.225]    [Pg.727]    [Pg.776]    [Pg.1350]    [Pg.1675]    [Pg.1837]   
See also in sourсe #XX -- [ Pg.325 ]

See also in sourсe #XX -- [ Pg.90 ]




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