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Production rate definition

Figure 7.17 shows a summary of the available conditions of water electrolysis [72]. For each configuration there exists a range of performance. Conventional electrolyzers, which nevertheless are still the most common in the current production of H 2 on the intermediate and small scale, show high overpotential and a relatively small production rate. Membrane (SPE) and advanced alkaline electrolyzers show very similar performance, with somewhat lower overpotential but a much higher production rate. Definite improvements in energy consumption would come from high temperature (steam) electrolysis, which is, however, still far from optimization because of a low production rate and problems of material stability. [Pg.265]

Static and Flexible Budgets Overhead cost can significantly affect the profitability of a projec t and is the only cost outside the control of the project manager. The project is expected to contribute a definite amount toward the expenses of the company and will be charged this amount even if the production rate is zero. This is the fixecTcomponent of the overhead cost and will include directly allocable costs such as depreciation and a proportion of general costs such as office salaries and heating. [Pg.857]

Many pubhcahons refer to the use of micro reactors for process intensificahon, with all the imphcahons related to this definition - safety, cost reduchon, high productivity rate, environmental friendliness, energy efficiency and so on [5, 25, 104]. A particular feature of interest is the reduction of the equipment size (see also Section 1.4.3.5 for a systematic top-down description of this topic). [Pg.57]

Both Rajdistr andR are introduced here as fines production rates with the dimension kg/s, which is in contrast to the definition of the overall attrition rate defined in Eqs. (2) and (3). [Pg.457]

The development of a quantitative theory of a free-radical copolymerization implies the derivation of equations for the rate of the monomers depletion and the statistical characteristics of the chemical structure of macromolecules present in the reaction system at the given conversion p of monomers. Elaborating such a theory one should take into account a highly important peculiarity inherent to any free-radical copolymerization. This peculiarity is that the characteristic time of a macroradical life is appreciably less than the time of the process duration. Consequently, its products represent definitely... [Pg.183]

Following the reaction rate definition of the form given in eq. (3.1), if component i is a reaction product the rate is positive if it is a reactant that is being consumed, the rate is negative thus, the rate of disappearance of the reactant is -r,. In environmental applications, as we are interested in the disappearance of a pollutant, the rate is expressed as -r, which is positive. The rate of disappearance is used in Chapters 3 and 5, where for simplicity it is referred to as the reaction rate. [Pg.58]

Fossil fuel, like oil, coal, and gas, which takes care of more than 90% of industry s energy needs, is not renewable on this time scale, at least if we adhere to the definition that a fuel is not renewable when its consumption rate exceeds its production rate. With fossil fuel so prominent in our industrial society, let us make a thermodynamic analysis of a fossil-fueled power station. [Pg.211]

Table 8.1 describes the steps of the methodology in more detail. The procedure starts with the Problem definition production rate, chemistry, product specifications, safety, health and environmental constraints, physical properties, available technologies. Then, a first evaluation of feasibility is performed by an equilibrium design. This is based on a thermodynamic analysis that includes simultaneous chemical and physical equilibrium (CPE). The investigation can be done directly by computer simulation, or in a more systematic way by building a residue curve map (RCM), as explained in the Appendix A. This step will identify additional thermodynamic experiments necessary to consolidate the design decisions, mainly phase-equilibrium measurements. Limitations set by chemical equilibrium or by thermodynamic boundaries should be analyzed here. [Pg.233]

Stage IV Declining Rate. Definition. The declining rate stage is defined as a period of decreasing rate of reaction which tends to approach a limit in the amount of reactant consumed, or product produced (zero rate), under the prevailing conditions of temperautre, irradiance, partial pressure of oxygen, concentration of reactants, etc. [Pg.329]

In catalysed reactions it is often more convenient to define the production rate per unit volume of catalyst or even per unit mass of catalyst, instead of the production per unit volume reaction volume. Eqn. (8.2) expresses the relations between the various rate definitions ... [Pg.386]

There are no detailed recommendations for analytical procedures in the field of biotechnological production of drugs, in contrast to the recommendations made by the FDA for bioanalytical methods [16], The absence of detailed guidelines for analytical method validation in this field is surprising. It is important to validate the quantification of both substrate and product during the process, at definite time intervals, to ensure proper calculation of the kinetics of the process i.e., the coefficients of substrate conversion, and production rates must be adequately calculated. The aim of the study in pa-... [Pg.39]

We can also assume that the cycle time is equal to the time between the moment when the concentration of the first component exceeds a certain threshold, i.e., 1 X 10 M, or 1 X 10 mg/mL, and imtil the concentration of the second component becomes smaller than the same threshold [3-7]. This definition gives smaller values of the cycle time i.e., the corresponding production rate is larger), which depend on the resolution between the two bands, i.e., on most... [Pg.852]

The specific production, the production rate, and the recovery yield are used for the definition of objective functions. [Pg.857]

For the definition of the cycle time, they considered the time required for regeneration and re-equilibration of the column after each nm. Assuming that j column volumes of solvent are needed to regenerate the column, the cycle time will be defined as the analytical retention time of the more retained component plus j times the void time. With this definition, the production rate can be expressed as ... [Pg.868]

The complete definition of column performance when the number of stages and feed location are fixed requires two specifications (Section 5.2.2). In studying the effect of reflux ratio on separation, other parameters, including product rates, are assumed constant. In Y-X graphical representation, a fixed product rate is implied by fixing the 7-line slope. This slope depends on the feed thermal conditions at feed tray temperature and pressure (Section 5.2.2). The column pressure is fixed, but its temperature depends on the product rates. Therefore, in order to maintain a fixed product rate, the (/-line slope must be held constant. The actual product rates corresponding to a given (/-line slope are calculated by material balance once the product compositions have been determined. [Pg.220]

The definition of minimum reflux is linked to a specification of separation between two components. In multi-component mixtures, the specified components are the light key and the heavy key components. Minimum reflux is meaningless if the column is specified in a manner that does not define a particular separation between two components, such as a specification of the number of trays and a product rate. Also, minimum reflux in this context is associated with singlefeed, two-product columns. For a given feed composition, the minimum reflux depends on the key components, their separation specification, and the feed thermal conditions. [Pg.399]

This method also considers the stage temperatures as the independent variables. The algorithm is applied to a single-feed, two-product column with a partial condenser and reboiler. As in the original Thiele-Geddes method, the problem definition is such that the feed component flow rates, are known and fixed. The column pressure profile is also fixed, as well as its configuration, which defines the number of stages and feed location. In addition, one product rate (the distillate) and one internal flow (such as the reflux rate, Lj) are specified. The solution method, outlined below, is described in detail by Holland (1975). [Pg.443]


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See also in sourсe #XX -- [ Pg.853 ]




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