Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Recycle compressor

However, many differences arise among the schemes when looking at how production rate is set and how liquid level and pressure in the reactor are controlled. For example, production rate is set in various strategies via fresh feed Fo0 flow, condenser cooling water flow, separator liquid flow, stripper base flow, or fresh feed FoC flow. Reactor level is controlled by fresh feeds FoD and F,lK, separator temperature setpoint, compressor recycle valve, or fresh feed FoC flow. Reactor pressure is controlled by reactor cooling water flow, purge flow, or FcA feed flow. In one strategy reactor pressure is uncontrolled and allowed to float. [Pg.253]

McCandless, F.P., A comparison of membrane cascades, some one compressor recycle permeators, and distillation. Journal of Membrane Science, 1994, 89(1 2) 51 72. [Pg.326]

In a plant producing liquid chlorine, the compressed gas goes next to the liquefaction system. Rather than impose a pressure drop between the processes, the gas is allowed to flow freely into liquefaction. A valve on the uncondensed gas venting from the liquefaction unit (Section 9.1.7.2) controls the pressure on both systems. When chlorine is sent to another process without liquefaction, it would be possible to withdraw it on downstream pressure control and let the compressor outlet pressure fluctuate. This approach leads to variability in the differential pressure across the compressor recycle valve. Fluctuations in this flow can cause fluctuations in the compressor suction pressure and therefore in the cellroom chlorine header. It is better to control the compressor outlet pressure itself, even at the cost of another pressure control loop at the destination. Section 11.3.2.6 describes instrumentation hardware and the problems of transferring chlorine to more than one destination. [Pg.822]

When the compressor first operates, the incoming pressure is well above the suction set point, and the valve upstream of the suction knockout pot (PV-1/200) must throttle the flow. As the line pressure falls, the valve continues to open. When it is wide open and can no longer hold the desired suction pressure, the compressor recycle valve (PV-2/200) must open. Finally, at some level of vacuum on the source, the system reaches its limits and can no longer pull chlorine from the container. Then comes shutdown. [Pg.1133]

Reactor Furnace Heat Exchanger Feed Mixer Quench Separator Compressor Recycle Column Stabilizer Column Product Column Entire flowsheet ... [Pg.387]

Because we require a pure product, a separator is needed. The unreacted FEED is usually too valuable to be disposed of and is therefore recycled to the reactor inlet via a pump or compressor (see Fig. 4.16). In addition, disposal of unreacted FEED rather than recycling creates an environmental problem. [Pg.96]

In the case of a liquid recycle, the cost of this pressure increase is usually small. Pumps usually have low capital and operating costs relative to other plant items. On the other hand, to increase the pressure of material in the vapor phase for recycle requires a compressor. Compressors tend to have a high capital cost and large power requirements giving higher operating costs. [Pg.115]

Sometimes it is extremely difficult to avoid vapor recycles without using very high pressures or very low levels of refrigeration, in which case we must accept the expense of a recycle compressor. However, when synthesizing the separation and recycle configuration, vapor recycles should be avoided, if possible, and liquid recycles used instead. [Pg.115]

The effluent from the reactor contains both PRODUCT and unreacted FEED which must be separated in a distillation column. Unreacted FEED is recycled to the reactor via a pump if the recycle is liquid or a compressor if the recycle is vapor. [Pg.241]

The unit has virtually the same flow sheet (see Fig. 2) as that of methanol carbonylation to acetic acid (qv). Any water present in the methyl acetate feed is destroyed by recycle anhydride. Water impairs the catalyst. Carbonylation occurs in a sparged reactor, fitted with baffles to diminish entrainment of the catalyst-rich Hquid. Carbon monoxide is introduced at about 15—18 MPa from centrifugal, multistage compressors. Gaseous dimethyl ether from the reactor is recycled with the CO and occasional injections of methyl iodide and methyl acetate may be introduced. Near the end of the life of a catalyst charge, additional rhodium chloride, with or without a ligand, can be put into the system to increase anhydride production based on net noble metal introduced. The reaction is exothermic, thus no heat need be added and surplus heat can be recovered as low pressure steam. [Pg.77]

Stripping of acetylene from the solvent takes place at atmospheric pressure. Pure acetylene is removed from the side of the stripper light impurities are removed overhead and recycled to the compressor. Higher acetylenes are removed from the side of a vacuum stripper with the acetylene overheads being recycled to the bottom of the acetylene stripper. [Pg.390]

Maleic anhydride in the product stream is removed and converted to a maleic acid solution in a water scmbbing system. The maleic acid is sent to the hydrogenation to produce THF while the reactor off-gas after scmbbing is sent to the recycle compressor. A small purge stream is sent to incineration. [Pg.457]

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]

Fig. 12. Unipol PP process where A is the polymerization reactor B, recycle gas compressor C, recycle gas cooler D, product discharge tank E, impact copolymer reactor F, recycle gas compressor G, recycle gas cooler and H, product discharge tank (134). Fig. 12. Unipol PP process where A is the polymerization reactor B, recycle gas compressor C, recycle gas cooler D, product discharge tank E, impact copolymer reactor F, recycle gas compressor G, recycle gas cooler and H, product discharge tank (134).
Propane and light ends are rejected by touting a portion of the compressor discharge to the depropanizer column. The reactor effluent is treated prior to debutanization to remove residual esters by means of acid and alkaline water washes. The deisobutanizer is designed to provide a high purity isobutane stream for recycle to the reactor, a sidecut normal butane stream, and a low vapor pressure alkylate product. [Pg.46]

Dehydration. Use of molecular sieve driers for final clean-up of the carbon oxides and water in the synthesis gas to less than 1 ppm levels has gained prominence in low energy ammonia plant designs. The sieves are usually located at the interstage of the synthesis gas compressor to reduce volume requirements. The purified make-up gas can then be combined with the recycle and routed direcdy to the converter. [Pg.350]

This ammonia is recycled to the reactor via a compressor and a heater. Liquid ammonia is used as reflux on the top of the absorber. The net amount of carbon dioxide formed in the reactor is removed as bottom product from the absorber in the form of a weak ammonium carbamate solution, which is concentrated in a desorber-washing column system. The bottom product of this washing column is a concentrated ammonium carbamate solution which is reprocessed in a urea plant. The top product, pure ammonia, is Hquefted and used as reflux together with Hquid makeup ammonia. The desorber bottom product, practically pure water, is used in the quench system in addition to the recycled mother Hquor. [Pg.373]

The major difficulty with these reactors is in the outside recycle pump, especially at high temperatures. Reciprocating pumps require seal rings, and these cannot take the high temperature needed for most reactions. If the recycle gas is cooled down before entering the compressor, it must be reheated before it enters the reactor again. This makes them complicated in construction and excessive in cost. [Pg.46]

The first objective of the antisurge control system is to protect the compressor. This can be accomplished for some disturbances by using the PI algorithm with a large value of bj. However, it is also necessary to maximize the region in which the compressor can operate with the recycle valve closed. This increases the efficiency of the compressor at lower throughputs. Steady-state operation with recycle is extremely inefficient. Therefore, from this perspective, small values of bj are highly desirable. [Pg.394]

Recycles are meticulously accounted for because they load equipment and draw utilities. An olefin plant sustaining relatively low conversion per pass often builds up large amounts of unreacted feed that is recycled to the steam crackers. With utilities charged to ultimate products, these recycles would seem to the model to be free. The model would likely opt for very low conversion, which usually gives high ultimate yield and saves feedstock. Assigning the utility costs to users causes the compressor to pay for the extra recycle and the model raises conversion to the true optimum value. [Pg.347]

FITK Mixer for feed and recycle PBC Product B to compressor... [Pg.348]


See other pages where Recycle compressor is mentioned: [Pg.186]    [Pg.1244]    [Pg.19]    [Pg.250]    [Pg.186]    [Pg.1244]    [Pg.19]    [Pg.250]    [Pg.121]    [Pg.242]    [Pg.68]    [Pg.361]    [Pg.503]    [Pg.391]    [Pg.373]    [Pg.373]    [Pg.440]    [Pg.350]    [Pg.181]    [Pg.479]    [Pg.483]    [Pg.327]    [Pg.331]    [Pg.334]    [Pg.440]    [Pg.1551]    [Pg.1574]    [Pg.33]    [Pg.181]    [Pg.392]    [Pg.395]    [Pg.396]    [Pg.397]    [Pg.397]   
See also in sourсe #XX -- [ Pg.163 , Pg.164 ]




SEARCH



© 2024 chempedia.info