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Low-pressure separator

Pressure-tubes allow the separate, low-pressure, heavy-water moderator to act as a backup hesit sink even if there is no water in the fuel channels. Should this fail, the calandria shell ilsdf can contain the debris, with the decay heat being transferred to the water-filled shield tank around the core. Should the severe core damage sequence progress further, the shield tank and the concrete reactor vault significantly delay the challenge to containment. Furthermore, should core melt lead to containment overpressure, the concrete containment wall will leak and reduce the possibility of catastrophic structural failure (Snell, 1990). [Pg.405]

Different types of absorbers are used for absorption. The most simple unit is an absorbing tower with sprayed liquid, with countercurrent motions of the gas and liquid. The efficiency depends on the size of drops produced and on the uniformity of their distribution in the tower. The absorber should be equipped with a drop separator. Low pressure losses and simple design are the advantage of this type of equipment. [Pg.562]

Description The feed, either paraffinic or olefinic C -Cg fraction, is heated through heat exchangers and a furnace to the desired temperature. The vaporized feed is fed to the top of the aromatization reactor. There are two reactors in series are in operation, and the other two reactors are in regeneration or standby. The effluent from the bottom of the second reactor is fed to the aromatization feed/effluent heat exchanger. After the feed/effluent heat exchanger, the reactor effluent is further cooled by air coolers and trim coolers with cooling water and chilled water. This cold effluent is then sent to the aromatization effluent separator (low pressure) where the rich net gas stream is separated from the aromatic-rich liquid. [Pg.72]

The initiator f and chain transfer agent g can be metered into the ethylene stream as it enters the reactor or at various points within it. From the reactor the product stream h containing a mixture of unreacted ethylene, oils, waxes, and polyethylene proceeds to a two stage separation process. The product stream is initially let down into a high pressure separator 4 wherein the polyethylene precipitates and is drained off with some ethylene i to a low pressure separator 5. The low molecular weight oils and waxes remain in solution in the bulk of the ethylene, and this stream j is let down into a separate low pressure separator 6. Here the ethylene is stripped from the oils and waxes, which are discharged in waste stream k. The ethylene for recycle I proceeds to a cooler 7, from which it is piped to... [Pg.49]

Figure 3.8a shows the temperature-composition diagram for a minimum-boiling azeotrope that is sensitive to changes in pressure. This azeotrope can be separated using two columns operating at different pressures, as shown in Fig. 3.86. Feed with mole fraction of A Ufa)) of, say, 0.3 is fed to the high-pressure column. The bottom product from this high-pressure column is relatively pure B, whereas the overhead is an azeotrope with jcda = 0-8, jcdb = 0.2. This azeotrope is fed to the low-pressure column, which produces relatively pure A in the bottom and in the overhead an azeotrope with jcda = 0.6, jcdb = 0.4. This azeotrope is added to the feed of the high-pressure column. Figure 3.8a shows the temperature-composition diagram for a minimum-boiling azeotrope that is sensitive to changes in pressure. This azeotrope can be separated using two columns operating at different pressures, as shown in Fig. 3.86. Feed with mole fraction of A Ufa)) of, say, 0.3 is fed to the high-pressure column. The bottom product from this high-pressure column is relatively pure B, whereas the overhead is an azeotrope with jcda = 0-8, jcdb = 0.2. This azeotrope is fed to the low-pressure column, which produces relatively pure A in the bottom and in the overhead an azeotrope with jcda = 0.6, jcdb = 0.4. This azeotrope is added to the feed of the high-pressure column.
Simple conventional refining is based essentially on atmospheric distillation. The residue from the distillation constitutes heavy fuel, the quantity and qualities of which are mainly determined by the crude feedstock available without many ways to improve it. Manufacture of products like asphalt and lubricant bases requires supplementary operations, in particular separation operations and is possible only with a relatively narrow selection of crudes (crudes for lube oils, crudes for asphalts). The distillates are not normally directly usable processing must be done to improve them, either mild treatment such as hydrodesulfurization of middle distillates at low pressure, or deep treatment usually with partial conversion such as catalytic reforming. The conventional refinery thereby has rather limited flexibility and makes products the quality of which is closely linked to the nature of the crude oil used. [Pg.484]

First, the films separately are allowed to expand to some low pressure, t, and by Eq. IV-48 the free energy change is... [Pg.142]

The yellow solution was poured into 150 ml of water. After addition of 20 g of ammonium chloride and vigorous shaking, the layers were separated. The aqueous layer was extracted twice with diethyl ether. The combined solutions were dried over magnesium sulfate and concentrated in a water-pump vacuum. The residue was distilled at low pressure giving the desired carbinol, (b.p. 40°C/0.1 mmHg), n 1.5505 in 66-702 yield. A small viscous residue remained in the distillation flask. [Pg.80]

The enhanced concentration at the surface accounts, in part, for the catalytic activity shown by many solid surfaces, and it is also the basis of the application of adsorbents for low pressure storage of permanent gases such as methane. However, most of the important applications of adsorption depend on the selectivity, ie, the difference in the affinity of the surface for different components. As a result of this selectivity, adsorption offers, at least in principle, a relatively straightforward means of purification (removal of an undesirable trace component from a fluid mixture) and a potentially useflil means of bulk separation. [Pg.251]

The Gaudfrin disk filter is designed for only relatively low pressures of 100 kPa on average and it provides for cake washing in two stages, in two separate compartments within the same vessel. [Pg.405]

Spiral-wound modules are much more commonly used in low pressure or vacuum gas separation appHcations, such as the production of oxygen-enriched air, or the separation of organic vapors from air. In these appHcations, the feed gas is at close to ambient pressure, and a vacuum is drawn on the permeate side of the membrane. Parasitic pressure drops on the permeate side of the membrane and the difficulty in making high performance hollow-fine fiber membranes from the mbbery polymers used to make these membranes both work against hollow-fine fiber modules for this appHcation. [Pg.75]

Pervaporation operates under constraints similar to low pressure gas-separation. Pressure drops on the permeate side of the membrane must be small, and many prevaporation membrane materials are mbbery. For this reason, spiral-wound modules and plate-and-frame systems ate both in use. [Pg.75]

The most convenient mathematical method of describing pervaporation is to divide the overall separation processes into two steps, as shown in Figure 40. The first is evaporation of the feed Hquid to form a (hypothetical) saturated vapor phase on the feed side of the membrane. The second is permeation of this vapor through the membrane to the low pressure permeate side of the membrane. Although no evaporation actually takes place on the feed side of the membrane during pervaporation, this approach is mathematically simple and is thermodynamically completely equivalent to the physical process. The evaporation step from the feed hquid to the saturated vapor phase produces a separation, which can be defined (eq. 13) as the ratio of... [Pg.86]

Recycle and Polymer Collection. Due to the incomplete conversion of monomer to polymer, it is necessary to incorporate a system for the recovery and recycling of the unreacted monomer. Both tubular and autoclave reactors have similar recycle systems (Fig. 1). The high pressure separator partitions most of the polymers from the unreacted monomer. The separator overhead stream, composed of monomer and a trace of low molecular weight polymer, enters a series of coolers and separators where both the reaction heat and waxy polymers are removed. Subsequendy, this stream is combined with fresh as well as recycled monomers from the low pressure separator together they supply feed to the secondary compressor. [Pg.373]


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See also in sourсe #XX -- [ Pg.131 , Pg.149 , Pg.201 ]




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