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Necessary Stream

If the reaction is to be performed in a continuous setting, two separate sets of equipment are required and must be operated simultaneously. Compositions are then obtained by mixing the necessary streams belonging to each structure in the appropriate proportions. By comparison, if it is desired to perform the same task under batch conditions, an identical outcome may be achieved by two serial operations together with intermediate storage of material used in mixing processes. Hence, it may turn out that a single set of reactive equipment is sufficient to achieve the same result. [Pg.232]

Label all unit operations in general terms, such as mixer, separator, heater, and cooler. Each unit on your flowsheet should perform only one operation, even though in actual practice one machine may perform multiple operations in sequence. Add the necessary streams for water, soap, bleach, and air and list the components in all streams. [Pg.42]

Analogous effects are caused by the inappropriate use of utilities. Utilities are appropriate if they are necessary to satisfy the enthalpy imbalance in that part of the process. Above the pinch in Fig. 6.7a, steam is needed to satisfy the enthalpy imbalance. Figure 6.86 illustrates what happens if inappropriate use of utilities is made and some cooling water is used to cool hot streams above the pinch, say, XP. To satisfy the enthalpy imbalance above the pinch, an import of (Q mjj,+XP) is needed from steam. Overall, (Qcmin+AP) of cooling water is used. ... [Pg.168]

Figure 16.4a shows the grid diagram with a CP table for design above the pinch. Cold utility must not be used above the pinch, which means that hot streams must be cooled to pinch temperature by recovery. Hot utility can be used, if necessary, on the cold streams above the pinch. Thus it is essential to match hot streams above the pinch with a cold partner. In addition, if the hot stream is at pinch conditions, the cold stream it is to be matched with must also be at... [Pg.366]

Figure B.l shows a pair of composite curves divided into vertical enthalpy intervals. Also shown in Fig. B.l is a heat exchanger network for one of the enthalpy intervals which will satisfy all the heating and cooling requirements. The network shown in Fig. B.l for the enthalpy interval is in grid diagram form. The network arrangement in Fig. B.l has been placed such that each match experiences the ATlm of the interval. The network also uses the minimum number of matches (S - 1). Such a network can be developed for any interval, providing each match within the interval (1) satisfies completely the enthalpy change of a strearh in the interval and (2) achieves the same ratio of CP values as exists between the composite curves (by stream splitting if necessary). Figure B.l shows a pair of composite curves divided into vertical enthalpy intervals. Also shown in Fig. B.l is a heat exchanger network for one of the enthalpy intervals which will satisfy all the heating and cooling requirements. The network shown in Fig. B.l for the enthalpy interval is in grid diagram form. The network arrangement in Fig. B.l has been placed such that each match experiences the ATlm of the interval. The network also uses the minimum number of matches (S - 1). Such a network can be developed for any interval, providing each match within the interval (1) satisfies completely the enthalpy change of a strearh in the interval and (2) achieves the same ratio of CP values as exists between the composite curves (by stream splitting if necessary).
To avoid hydrate formation, it is necessary either to dry the stream, or to inject a substance that, dissolving the water, lowers its partial fugacity and, consequently, the temperature of hydrate formation. [Pg.174]

Before designing a process scheme it is necessary to know the specification of the raw material input (or feedstock) and the specification of the enc/procfucf desired. Designing a process to convert fluids produced at a wellhead into oil and gas products fit for evacuation and storage is no different. The characteristics of the well stream or streams must be known and specifications for the products agreed. [Pg.236]

The set-up of Fig. 11, 41, 3 ensures the complete condensation of the steam when a rapid flow of steam is necessary for satisfactory results, and is useful in the distillation of large volumes of liquids of low vapour pressure, such as nitrobenzene. Thus the flask A containing the mixture may be of 3-litre capacity and B may be a 1-litre flask the latter is cooled by a stream of water, which is collected in a funnel and conducted to the sink. The receiver C must be of proportionate size all stoppers... [Pg.147]

If undiluted diacetylene is required, the experiment can be carried out in the same way, but preferably on a smaller scale. 3 Traps should then be used and the stream of nitrogen should be slower. The boiling point of diacetylene is said to be about 10°C. The solutions of diacetylene probably can be stored (under nitrogen in the refrigerator) for at least 24 h without decomposition. Though explosions have never been experienced by the authors, it is advisable to handle diacetylene with the necessary respect. [Pg.148]

Nebulizers are used to introduce analyte solutions as an aerosol spray into a mass spectrometer. For use with plasma torches, it is necessary to produce a fine spray and to remove as much solvent as possible before the aerosol reaches the flame of the torch. Various designs of nebulizer are available, but most work on the principle of interacting gas and liquid streams or the use of ultrasonic devices to cause droplet formation. For nebulization applications in thermospray, APCI, and electrospray, see Chapters 8 and 11. [Pg.152]

For mass spectrometric analysis of an analyte solution using a plasma torch, it is necessary to break down the solution into a fine droplet form that can be swept into the flame by a stream of argon gas. On the way to the flame, the droplets become even smaller and can eventually lose all solvent to leave dry analyte particulate matter. This fine residual matter can be fragmented and ionized in the plasma flame without disturbing its operation. [Pg.400]

In the one-stage process (Fig. 2), ethylene, oxygen, and recycle gas are directed to a vertical reactor for contact with the catalyst solution under slight pressure. The water evaporated during the reaction absorbs the heat evolved, and make-up water is fed as necessary to maintain the desired catalyst concentration. The gases are water-scmbbed and the resulting acetaldehyde solution is fed to a distUlation column. The tad-gas from the scmbber is recycled to the reactor. Inert materials are eliminated from the recycle gas in a bleed-stream which flows to an auxdiary reactor for additional ethylene conversion. [Pg.52]

Specification tests are performed on plant streams once or twice per worker shift, or even more often if necessary, to assure the continuing quahty of the product. The tests are also performed on a sample from an outgoing shipment, and a sample of the shipment is usually retained for checking on possible subsequent contamination. Tests on specialty types of acetone may require sophisticated instmments, eg, mass spectrometry for isotopicaHy labeled acetone. [Pg.98]

Environmental Considerations. Environmental problems in Ziegler chemistry alcohol processes are not severe. A small quantity of aluminum alkyl wastes is usually produced and represents the most significant disposal problem. It can be handled by controlled hydrolysis and separate disposal of the aqueous and organic streams. Organic by-products produced in chain growth and hydrolysis can be cleanly burned. Wastewater streams must be monitored for dissolved carbon, such as short-chain alcohols, and treated conventionally when necessary. [Pg.457]


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