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Rate laws continued removal

This law can be applied to steady-state or unsteady-state (transient) processes and to batch or continuous reactor systems. A steady-state process is one in which there is no change in conditions (e.g., pressure, temperature, composition) or rates of flow with time at any given point in the system. The accumulation term in Equation (7.2) is then zero. (If there is no chemical or nuclear reaction, the generation term is also zero.) All other processes are unsteady-state. In a batch reactor process, a given quantity of reactants is placed in a container, and by chemical and/or physical means, a change is made to occur. At the end of the process, the container (or adjacent containers to which material may have been transferred) holds the product or products. In a continuous process, reactants are continuously removed from one or more points. A continuous process may or may not be steady-state. A coal-fired power plant, for example, operates continuously. However, because of the wide variation in power demand between peak and slack periods, there is an equally wide variation in the rate at which the coal is fired. For this reason, power plant problems may require the use of average data over long periods of time. However, most industrial operations are assumed to be steady-state and continuous. [Pg.128]

Between samples, the residual solute in the polymer is removed by continued exposure to back extractant. This process requires about 2 min for 1 mM sample solutions. As expected from diffusion laws, this time period for residual removal varies with the square of the sample concentrations. Higher sampling rates require keeping analyte concentrations below about 1 mM. [Pg.348]

Table IV summarizes the findings of such studies. The results of Sontag et al. have been confirmed many times, viz., the Mo/Al catalyst reduces slower than bulk Mo03. Whereas, bulk Mo03 reduction proceeds rapidly to MoO, then more slowly to Mo metal (22), no such sequence is observed for the catalyst (25). Further, despite occasional claims in the literature, reduction does not stop at the Mo02 state—more than one O/Mo is removed at high temperature, and considerably less than one O/Mo is removed at low temperature. In one case, it was reported that reduction continued even after 2 days (24). Fractional reduction increased with increase in the Mo content of the catalyst (16, 23, 25). Reduction rates have generally followed the Elovich law, indicative of a surface... Table IV summarizes the findings of such studies. The results of Sontag et al. have been confirmed many times, viz., the Mo/Al catalyst reduces slower than bulk Mo03. Whereas, bulk Mo03 reduction proceeds rapidly to MoO, then more slowly to Mo metal (22), no such sequence is observed for the catalyst (25). Further, despite occasional claims in the literature, reduction does not stop at the Mo02 state—more than one O/Mo is removed at high temperature, and considerably less than one O/Mo is removed at low temperature. In one case, it was reported that reduction continued even after 2 days (24). Fractional reduction increased with increase in the Mo content of the catalyst (16, 23, 25). Reduction rates have generally followed the Elovich law, indicative of a surface...
These laws (determined by Michael Faraday over a half century before the discovery of the electron) can now be shown to be simple consequences of the electrical nature of matter. In any electrolysis, an oxidation must occur at the anode to supply the electrons that leave this electrode. Also, a reduction must occur at the cathode removing electrons coming into the system from an outside source (battery or other DC source). By the principle of continuity of current, electrons must be discharged at the cathode at exactly the same rate at which they are supplied to the anode. By definition of the equivalent mass for oxidation-reduction reactions, the number of equivalents of electrode reaction must be proportional to the amount of charge transported into or out of the electrolytic cell. Further, the number of equivalents is equal to the number of moles of electrons transported in the circuit. The Faraday constant (F) is equal to the charge of one mole of electrons, as shown in this equation ... [Pg.328]

A vessel 1.0 m in diameter is to be used for stripping chloroform from water by sparging with air at 298 K. The water will flow continuously downward at the rate of 10.0 kg/s at 298 K. The water contains 240 pg/L of chloroform. It is desired to remove 90% of the chloroform in the water using an airflow that is 50% higher than the minimum required. At these low concentrations, chloroform-water solutions follow Henry s law (yj = mx) with m = 220. The sparger is in the form of a ring located at the bottom of the vessel, 50 cm in diameter, containing 90 orifices, each 3 mm in diameter. Estimate the depth of the water column required to achieve the specified 90% removal efficiency. Estimate the power required to operate the air compressor, if the mechanical efficiency of the system is 60%. [Pg.246]

But due to flotation (bubble-film extraction), the products of bacterial metabolism and the products of bacterial degradation together with other water contaminants are ranoved continuously from recirculation flow through the bubble-film extractor. As a result, another positive feedback is realized in filtration-flotation system. The essence of this effect lies in the inhibition of vital functions of bacteria with increasing microbial metabolite concentration according to the law of chemical kinetics. And in accordance with the same law, bacterial activity is increased as the products of bacterial metabolism are removed from treated water [20]. Thus, we are able to add one more component, namely, AK, to the magnitude (/fj + AK2). The component AK represents the increase in biofiltration efficiency due to bacterial inhibitors removed by means of bubble-film extraction. In such a way, the resulting rate constant of the process takes the form ( fi + AK2 + AKi). [Pg.503]

In a creep test a sample is placed under a constant stress, and strain is recorded as a function of time. If an ideal elastic solid is subjected to a creep test, it will exhibit an immediate elastic strain in accordance with Hooke s law, but the strain will remain constant thereafter until the stress is removed, when the sample will return elastically to zero strain. An ideal liquid responds to a creep test quite differently. There is no initial elastic response, and there will be a continuously increasing strain with a slope inversely proportional to the viscosity the strain rate wUl remain constant. When the stress is removed, there is no elastic recovery— the liquid simply stops flowing in other words, the strain rate returns to zero. [Pg.394]


See other pages where Rate laws continued removal is mentioned: [Pg.869]    [Pg.26]    [Pg.79]    [Pg.573]    [Pg.344]    [Pg.384]    [Pg.64]    [Pg.210]    [Pg.203]    [Pg.573]    [Pg.4]    [Pg.184]    [Pg.345]    [Pg.279]    [Pg.414]    [Pg.141]    [Pg.79]    [Pg.21]    [Pg.254]    [Pg.52]   
See also in sourсe #XX -- [ Pg.354 , Pg.355 ]




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