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Vaporizers design

To use the ECES system, activity coefficient data for FeCl2 had to be developed. A recent paper by Susarev et al (15) presented experimental results of the vapor pressure of water over ferrous chloride solutions for temperatures from 25 to 100°C and concentrations of 1 to 4.84 molal. This data was entered into the ECES system in the Data Preparation Block with a routine VAPOR designed to regress such data and develop the interaction coefficients B, C, D of our model. These results replaced an earlier entry which was based on more limited data. All other data for studying the equilibria in the FeCl2-HCl-H20 system was already contained within the ECES system. [Pg.242]

It is important to check that the design and operating heat flux is well below the critical flux. Several correlations are available for predicting the critical flux. That given by Zuber et al. (1961) has been found to give satisfactory predictions for use in reboiler and vaporizer design. In SI units, Zuber s equation can be written as... [Pg.895]

The TSP interface was developed in the laboratories of Vestal at the University of Houston. It was the result of a long-term research project which started in the mid-70 s, aiming at the development of an LC-MS interface which is compatible with 1 ml/min of aqueous mobile phase and capable to provide both El and solvent-independent Cl [62]. The initial interface was a highly complex system, which subsequently was greatly simplified with respect to vaporizer design and vacuum system [58, 62-65]. Developments in vaporizer design are summarized in Table 4.1. Finally, direct electrically-heated vaporizers were applied [64-65]. [Pg.84]

Are carbynes produced in laboratory carbon and C IC Ar vapors designed to simulate the properties carbon dust in astrophysical environments Field-emission scanning electron microscope (FESEM) and HRTEM studies of vapor-condensed carbon smokes showed a wide range of carbon morphologies that were free of metal impurities (at EDS detection limits), viz. 1. Ceo and higher fullerenes that agglomerated into amorphous soot grains, 2. fullerenic nanotubes and onions, 3. amorphous carbon sheets,... [Pg.357]

Ao represents physical equilibrium. It places a limit on the possible accumulation of NCI3 and is independent of vaporizer design. The term kxjp in the denominator shows the influence of vaporizer design and process conditions. [Pg.924]

In Equation (24), a is the estimated standard deviation for each of the measured variables, i.e. pressure, temperature, and liquid-phase and vapor-phase compositions. The values assigned to a determine the relative weighting between the tieline data and the vapor-liquid equilibrium data this weighting determines how well the ternary system is represented. This weighting depends first, on the estimated accuracy of the ternary data, relative to that of the binary vapor-liquid data and second, on how remote the temperature of the binary data is from that of the ternary data and finally, on how important in a design the liquid-liquid equilibria are relative to the vapor-liquid equilibria. Typical values which we use in data reduction are Op = 1 mm Hg, = 0.05°C, = 0.001, and = 0.003... [Pg.68]

In modern separation design, a significant part of many phase-equilibrium calculations is the mathematical representation of pure-component and mixture enthalpies. Enthalpy estimates are important not only for determination of heat loads, but also for adiabatic flash and distillation computations. Further, mixture enthalpy data, when available, are useful for extending vapor-liquid equilibria to higher (or lower) temperatures, through the Gibbs-Helmholtz equation. ... [Pg.82]

Partially vaporized feed reverses these effects. For a given separation, the feed conditions can be optimized. No attempt should be made to do this at this stage in the design, since heat integration is likely to change the optimal setting later in the design. It is usually adequate to set the feed to saturated liquid conditions. This tends to equalize the vapor rate below and above the feed. [Pg.78]

In preliminary process design, the primary consideration is contact by inhalation. This happens either through accidental release of toxic material to the atmosphere or the fugitive emissions caused by slow leakage from pipe flanges, valve glands, and pump and compressor seals. Tank filling causes emissions when the rise in liquid level causes vapor in the tank to be released to the atmosphere. [Pg.259]

The problem with the fiowsheet shown in Fig. 10.5 is that the ferric chloride catalyst is carried from the reactor with the product. This is separated by washing. If a reactor design can be found that prevents the ferric chloride leaving the reactor, the effluent problems created by the washing and neutralization are avoided. Because the ferric chloride is nonvolatile, one way to do this would be to allow the heat of reaction to raise the reaction mixture to the boiling point and remove the product as a vapor, leaving the ferric chloride in the reactor. Unfortunately, if the reaction mixture is allowed to boil, there are two problems ... [Pg.285]

As shown in Fig. 10.6, the vapor from the reactor flows into the bottom of a distillation column, and high-purity dichloroethane is withdrawn as a sidestream several trays from the column top. The design shown in Fig. 10.6 is elegant in that the heat of reaction is conserved to run the separation and no washing of the reactor... [Pg.286]

Both the reboiling and condensing processes normally take place over a range of temperature. Practical considerations, however, usually dictate that the heat to the reboiler must be supplied at a temperature above the dew point of the vapor leaving the reboiler and that the heat removed in the condenser must be removed at a temperature lower than the bubble point of the liquid. Hence, in preliminary design at least, both reboiling and condensing can be assumed to take place at constant temperatures. ... [Pg.341]

Establish simple sequences. Using methods described in Chap. 5, sequences of simple columns with low overall vapor load are established. Consideration should not be restricted to the single sequence with the lowest overall vapor load, since many factors need to be considered in finally arriving at the best design. [Pg.348]

As pointed out in Chap. 5, replacing simple columns by complex columns tends to reduce the vapor (and heat) load but requires more of the heat to be added or removed at extreme levels. This means that the introduction of complex columns in the design might prejudice heat integration opportunities. Thus the introduction of complex distillation arrangements needs to be considered simultaneously with the heat integration. This can be carried out manually with some trial and error or using an automated procedure such as that of Kakhu and Flower. ... [Pg.349]

In the standard method, the metal enclosure (called the air chamber) used to hold the hydrocarbon vapors is immersed in water before the test, then drained but not dried. This mode of operation, often designated as the wet bomb" is stipulated for all materials that are exclusively petroleum. But if the fuels contain alcohols or other organic products soluble in water, the apparatus must be dried in order that the vapors are not absorbed by the water on the walls. This technique is called the dry bomb" it results in RVP values higher by about 100 mbar for some oxygenated motor fuels. When examining the numerical results, it is thus important to know the technique employed. In any case, the dry bomb method is preferred. [Pg.189]

For optimum combustion, the fuel should vaporize rapidly and mix intimately with the air. Even though the design of the injection system and combustion chamber play a very important role, properties such as volatility, surface tension, and fuel viscosity also affect the quality of atomization and penetration of the fuel. These considerations justify setting specifications for the density (between 0.775 and 0.840 kg/1), the distillation curve (greater than 10% distilled at 204°C, end point less than 288°C) and the kinematic viscosity (less than 8 mm /s at -20°C). [Pg.226]

It is important to keep in mind that the phases are mutually in equilibrium. In particular, the designation is a reminder that the solid surface must be in equilibrium with the saturated vapor pressure and that there must therefore be an adsorbed film of film pressure (see Section X-3B). Thus... [Pg.353]

Schematic diagram of a thermospray ion. source. This source, of current design, also incorporates (a) a discharge electrode so that the source can be operated in plasmaspray mode and (h) a repeller electrode to induce fragmentation. The vaporizer itself can be used as a discharge electrode. Schematic diagram of a thermospray ion. source. This source, of current design, also incorporates (a) a discharge electrode so that the source can be operated in plasmaspray mode and (h) a repeller electrode to induce fragmentation. The vaporizer itself can be used as a discharge electrode.
These factors make it necessary to reduce the amount of solvent vapor entering the flame to as low a level as possible and to make any droplets or particulates entering the flame as small and of as uniform a droplet size as possible. Desolvation chambers are designed to optimize these factors so as to maintain a near-constant efficiency of ionization and to flatten out fluctuations in droplet size from the nebulizer. Droplets of less than 10 pm in diameter are preferred. For flow rates of less than about 10 pl/min issuing from micro- or nanobore liquid chromatography columns, a desolvation chamber is unlikely to be needed. [Pg.107]


See other pages where Vaporizers design is mentioned: [Pg.1441]    [Pg.225]    [Pg.31]    [Pg.126]    [Pg.119]    [Pg.1264]    [Pg.1679]    [Pg.9]    [Pg.1675]    [Pg.1445]    [Pg.180]    [Pg.45]    [Pg.211]    [Pg.271]    [Pg.845]    [Pg.246]    [Pg.1186]    [Pg.96]    [Pg.106]    [Pg.180]    [Pg.1441]    [Pg.225]    [Pg.31]    [Pg.126]    [Pg.119]    [Pg.1264]    [Pg.1679]    [Pg.9]    [Pg.1675]    [Pg.1445]    [Pg.180]    [Pg.45]    [Pg.211]    [Pg.271]    [Pg.845]    [Pg.246]    [Pg.1186]    [Pg.96]    [Pg.106]    [Pg.180]    [Pg.111]    [Pg.147]    [Pg.166]    [Pg.335]    [Pg.350]    [Pg.358]    [Pg.359]    [Pg.526]    [Pg.1910]    [Pg.428]   


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