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Product specification calculation

Similarly a hypothetical spHtter must be defined when a stream is spHt. Furthermore, control units ate identified in calculations flow diagrams when temperatures, pressures, and flows of streams ate controlled on the basis of variables in other parts of flow sheets. Sometimes variables such as product specifications and reactor yields can be represented as hypothetical control units. [Pg.73]

The control system requires the values of T and AT obsei-ved during the first minutes of operation to be stored as the basis for the above calculation of end point. When the exhaust temperature then reaches the value calculated, diying is terminated. Coefficient K can be estimated from models but requires adjustment on-hne to reach product specifications repeatedly. Products having different moisture specifications or particle size will require different settings of K, but the system does compensate for variations in feed moisture, batch size, air moisture, and inlet temperature. Some exhaust air may be recirculated to control the dewpoint of the inlet air, thereby consei-v-ing energy toward the end of the batch and when the ambient air is especially diy. [Pg.751]

The MRLs are derived from data from supervised residue trials that are generally carried out in the context of food production. Specific conditions of feed production are not considered. Therefore, many practical problems for the official control of feed must be solved in future, e.g., application of transfer factors and the calculation of MRLs for mixed feed. [Pg.18]

If the composition (or flow-rate) of one stream is fixed by internal or external constraints, this may fix the composition and flows of other process streams. In Chapter 1, the relationship between the process variables, the design variables and design equations was discussed. If sufficient design variables are fixed by external constraints, or by the designer, then the other stream flows round a unit will be uniquely determined. For example, if the composition of one product stream from a distillation column is fixed by a product specification, or if an azeotrope is formed, then the other stream composition can be calculated directly from the feed compositions see Section 2.10. The feed composition would be fixed by the outlet composition of the preceding unit. [Pg.144]

Equation (5) is equivalent to stating that sublimation and subsequent transport of 1 g of water vapor into the chamber demands a heat input of 650 cal (2720 J) from the shelves. The vial heat transfer coefficient, Kv, depends upon the chamber pressure, Pc and the vapor pressure of ice, P0, depends in exponential fashion upon the product temperature, Tp. With a knowledge of the mass transfer coefficients, Rp and Rs, and the vial heat transfer coefficient, Kv, specification of the process control parameters, Pc and 7 , allows Eq. (5) to be solved for the product temperature, Tp. The product temperature, and therefore P0, are obviously determined by a number of factors, including the nature of the product and the extent of prior drying (i.e., the cake thickness) through Rp, the nature of the container through Kv, and the process control variables Pc and Ts. With the product temperature calculated, the sublimation rate is determined by Eq. (4). [Pg.632]

In the second section of the AP exam, you should begin all questions by numbering your answer. You do not need to work the questions in order. However, the graders must be able to identify quickly which question you are answering. You may wish to underline any key words or key concepts in your answer. Do not underline too much, however, because doing so may obscure your reasons for underlining. In free-response questions that require specific calculations or the determination of products, you may also want to underline or draw a box around your final answer(s). [Pg.26]

Monthly capital costs for transit inventories are calculated based on the transportation lane and product-specific transit inventory value in the basis currency of the end location and applying the interest rate equation. [Pg.179]

The Stoner product (30), calculated across the actinide series for homologous compounds, may interpret (or predict) the magnetic behaviour of these solids, and hence suggest a localized or itinerant picture (see Chap. D), provided that we know I for the different actinides across the series, since N(pf) is measurable (e.g. through specific heat measurements) and roughly reciprocal to the bandwidth W (N(pf) W ). I is not directly measurable and must be calculated. (Of course, the discussion above shows that the two quantities are not really independent, since the interactions determining I also play a role in determining the bandwidth, and hence N([Xf).)... [Pg.37]

Problem 7.20 Optically pure (S)-(-i-)-CH3CHBr-n-CjH,3 has [a] = -1-36.0°. A partially racemized sample having a specific rotation of -i-30° is reacted with dilute NaOH to form (R)-(-)-CH,CH(OH)-n-CsH,3 ([ ] =-5. 97°), whose specific rotation is -10.3° when optically pure, (a) Write an equation for the reaction using projection formulas, (b) Calculate the percent optical purity of reactant and product, (c) Calculate percentages of racemization and inversion, (d) Calculate percentages of frontside and backside attack, (e) Draw a conclusion concerning the reactions of 2° alkyl halides. (/) What change in conditions would increase inversion ... [Pg.125]

Mass-balance calculations for the first 3 years of acid additions indicate that the principal IAG processes are sulfate reduction and cation production. Specifically, one-third of the total sulfate input (added acid and deposition) was neutralized by in-lake processes. Increased sulfate reduction consumed slightly more than one-sixth and production of cations neutralized somewhat less than one-sixth of the acid added. Of the remaining sulfate, one-third was lost by outflow, and one-third decreased lake alkalinity. Laboratory determinations suggest that sediment-exchange processes occurring in only the top 2 cm of surficial sediments can account for the observed increase in water-column cations. Acidification of the near-surface sediments (with partial loss of exchangeable cations) will slow recovery because of the need to exchange the sediment-bound H+ and neutralize it by other processes. Reactor-based models that include the primary IAG processes predict that... [Pg.161]

Formulation of the mathematical model here adopts the usual assumptions of equimolar overflow, constant relative volatility, total condenser, and partial reboiler. Binary variables denote the existence of trays in the column, and their sum is the number of trays N. Continuous variables represent the liquid flow rates Li and compositions xj, vapor flow rates Vi and compositions yi, the reflux Ri and vapor boilup VBi, and the column diameter Di. The equations governing the model include material and component balances around each tray, thermodynamic relations between vapor and liquid phase compositions, and the column diameter calculation based on vapor flow rate. Additional logical constraints ensure that reflux and vapor boilup enter only on one tray and that the trays are arranged sequentially (so trays cannot be skipped). Also included are the product specifications. Under the assumptions made in this example, neither the temperature nor the pressure is an explicit variable, although they could easily be included if energy balances are required. A minimum and maximum number of trays can also be imposed on the problem. [Pg.6]

This section discusses the design of a suitable absorption column for the production of nitric acid by the single-pressure process. A comprehensive design study determined the column mechanical details and physical characteristics, together with its anticipated performance. This chapter contains the operating criteria and product specifications, the solution method, and finally the results of the design calculations. Details of the design calculations and all associated data are included in Appendix G. [Pg.163]

Neat isopropyl methylphosphinate (1) reacts exothermically on dropwise addition to methyl triflate to form a phosphonium salt (2), NMR 6 +73.4 (downfield from external H,P0.) J = 656 Hz, which yields isopropyl methyl methylphosphonite (3), when slowly added to a cold benzene solution containing excess tri-ethylamine (TEA). On warming to room temperature, the product was obtained as a benzene/TEA solution, which separated from a heavier liquid layer that consisted mainly of amine salt byproducts in benzene/TEA. When (R)-(+)-l (25% enantiomorphic excess) was used, a solution of (R)-(+)-3 (5 +176.6) was obtained in 60% yield, 90 mole-% pure with respect to its organophosphorus content. 2(Pie specific rotation of this product was calculated to be [a]D + 67.7 (c 2.6, benzene), if optically pure (+)-l starting material... [Pg.558]

The initial specific rates of 02 consumption and C02 production are calculated and interpreted, and the effect of diminishing 02 concentration on its specific consumption rate is investigated. For each test type, the mean and standard deviation of the 02 and C02 specific rates are calculated and tabulated in Table 1. The four types of stoppered culture tests were compared using two-sample t tests on these quantities to determine whether the particular conditions affected the cell metabolism [74]. If either initial rate showed a statistically significant (95 % confidence level) difference between the two test types being compared, then we concluded that the conditions affected metabolism and would be likely to affect bioreactor performance. [Pg.43]

Once the optimal batch time is obtained, the corresponding optimal reflux ratio and the maximum achievable conversion can be calculated directly using the polynomial equations presented in Figure 9.9 and 9.11, respectively. For frequently changed market prices, the same methodology can be applied efficiently without any difficulties to find the optimal batch time, amount of products, energy costs, etc. to calculate the maximum attainable profit. However, note the same exercise will have to be carried out for each product specification (x D). [Pg.286]

The calculation of the flame temperature for a combustible gas like hydrogen, carbon monoxide, or methane at first sight appears to be a simple problem since the apparently necessary data are only the heat of combustion and the specific heats of the products. Such calculations always yield very high results much above those recorded by direct experimental measurements. The discrepancy is probably due to a combination of several causes. On account of the temperature of the flame the products are partially dissociated,1 so that combustion is not complete m the flame. The specific heat of gases increases with rise m temperature, so that the value obtained at the ordinary temperature for the specific heat is too low. In addition to these two causes, another contributory factor is the loss of heat by radiation, which may be very considerable even m nou-lummous flames, whilst the general presence of an excess of the supporter of combustion and the non-instantaneous character of the combustion also detract from the accuracy of the calculation.2... [Pg.82]

Sample login involves registering a sample with the system by assigning, either manually or automatically, a unique identification called the sample ID. During this process, a "snapshot" of the product specification, test and calculation dictionaries is taken by moving all required information into the database, as defined in the configuration tables. This login process can be performed by a remote computer as well. [Pg.25]

Failure to have an adequate validation procedure for computerized spreadsheets used for in-process and finished product analytical calculations. The current validation procedure uses only the values that result in within specification findings, aberrant high findings, and aberrant low findings [21 CFR 211.165(e)]. For example, SOP 644.00, QA/QC Spreadsheet Validation, is deficient in that only a small range of values are being used to challenge computerized spreadsheet mathematical calculations. [Pg.741]

In the recent years Simulated Moving Bed (SMB) technology has become more and more attractive for complex separation tasks. To ensure the compliance with product specifications, a robust control is required. In this work a new optimization bas adaptive control strategy for the SMB is proposed A linearized reduced order model, which accounts for the periodic nature of the SMB process is used for online optimization and control purposes. Concentration measurements at the raffinate and extract outlets are used as the feedback information together with a periodic Kalman filter to remove model errors and to handle disturbances. The state estimate from the periodic Kalman filter is then used for the prediction of the outlet concentrations over a pre-defined time horizon. Predicted outlet concentrations constitute the basis for the calculation of the optimal input adjustments, which maximize the productivity and minimize the desorbent consumption subject to constraints on product purities. [Pg.177]

The range of sterilization specifications calculable by these various approaches is summarized in Table 2. It is apparent that very brief sterilization specifications (on the order of 2-3 min holding time at 121°C) are obtainable when the microbiological contamination is completely characterized in terms of numbers and thermal resistances. In practice, such limits on hold times could be difficult to control precisely, are probably insignificant in terms of thermal lethality compared with heat-up and cool-down times, and could prove difficult to sell to regulators. Without complete thermal characterization of thermal resistances, specifications calculable by the bioburden approach are hardly significantly shorter than overkill specifications. Thus, it probably makes practical sense in most cases to choose only between overkill cycles for thermally resistant products and aseptic manufacture for heat-sensitive products. [Pg.328]

The results of endotoxin tests for in-process solutions, bulk materials, and finished parenteral products should be reported in the same units as those assigned to the product. Two factors determine the sensitivity of a BET. For infusion solutions and device extracts, the gel-clot sensitivity or the lowest point on the standard curve (lambda for kinetic LAL) and the amount of dilution determine test sensitivity.For products that have an endotoxin limit in EU/mg, the choice of lambda and the concentration of the test material determine sensitivity. The formula for product-specific sensitivity (PSS) is a convenient way to calculate the sensitivity of a BET for this type of product, where ... [Pg.3061]


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See also in sourсe #XX -- [ Pg.168 ]




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