Big Chemical Encyclopedia

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

Articles Figures Tables About

Recycled gas

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]

Use a recycle gas or recycle the pollutants rather than using fresh air or venting. [Pg.385]

The feed to the arc consists of a mixture of fresh hydrocarbons and recycle gas. Table 6 indicates the composition of a typical feedstock as well as the composition of the gas leaving the arc furnace. [Pg.385]

Ethylene Stripping. The acetylene absorber bottom product is routed to the ethylene stripper, which operates at low pressure. In the bottom part of this tower the loaded solvent is stripped by heat input according to the purity specifications of the acetylene product. A lean DMF fraction is routed to the top of the upper part for selective absorption of acetylene. This feature reduces the acetylene content in the recycle gas to its minimum (typically 1%). The overhead gas fraction is recycled to the cracked gas compression of the olefin plant for the recovery of the ethylene. [Pg.391]

Fresh butane mixed with recycled gas encounters freshly oxidized catalyst at the bottom of the transport-bed reactor and is oxidized to maleic anhydride and CO during its passage up the reactor. Catalyst densities (80 160 kg/m ) in the transport-bed reactor are substantially lower than the catalyst density in a typical fluidized-bed reactor (480 640 kg/m ) (109). The gas flow pattern in the riser is nearly plug flow which avoids the negative effect of backmixing on reaction selectivity. Reduced catalyst is separated from the reaction products by cyclones and is further stripped of products and reactants in a separate stripping vessel. The reduced catalyst is reoxidized in a separate fluidized-bed oxidizer where the exothermic heat of reaction is removed by steam cods. The rate of reoxidation of the VPO catalyst is slower than the rate of oxidation of butane, and consequently residence times are longer in the oxidizer than in the transport-bed reactor. [Pg.457]

Quench Converter. The quench converter (Fig. 7a) was the basis for the initial ICl low pressure methanol flow sheet. A portion of the mixed synthesis and recycle gas bypasses the loop interchanger, which provides the quench fractions for the iatermediate catalyst beds. The remaining feed gas is heated to the inlet temperature of the first bed. Because the beds are adiabatic, the feed gas temperature increases as the exothermic synthesis reactions proceed. The injection of quench gas between the beds serves to cool the reacting mixture and add more reactants prior to entering the next catalyst bed. Quench converters typically contain three to six catalyst beds with a gas distributor in between each bed for injecting the quench gas. A variety of gas mixing and distribution devices are employed which characterize the proprietary converter designs. [Pg.279]

Tube-Cooled Converter. The tube-cooled converter functions as an interchanger, consisting of a tube-filled vessel with catalyst on the shell side (Fig. 7c). The combined synthesis and recycle gas enters the bottom of the reactor tubes, where it is heated by the reaction taking place in the surrounding catalyst bed. The gas turns at the top of the tubes and passes down through the catalyst bed. The principal advantage of this converter is in... [Pg.279]

PETROSIX. The PETROSIX technology is operated in the IH mode using hot recycle gas as the heat-transport medium. The PETROSIX retort has only one level of heat input, uses countercurrent flows, and uses a circular grate to control the flow of soflds (Eig. 3). The PETROSIX has been operated by Petrobras (Brazil) since the 1950s and is one of the few retorting processes producing shale oil in 1995. [Pg.348]

P r ho. The Paraho retorting technology is similar to the PETROSIX technology except that it can be operated in the direct heat (DH) mode. The unique feature of the Paraho technology is the two levels of heat input (Fig. 4). In the IH mode, the air blower shown in Figure 4 is replaced by a recycle gas heater. The Paraho DH operation has been carried out neat Rifle, Colorado since the 1970s operations to produce asphalt (qv) from shale oil are continuing. [Pg.349]

UNISHALE B. The UNISHALE process, like the Paraho process, uses lump feed and countercurrent flows, and can be operated ia either the DH or IH mode. The UNISHALE B process is an IH process that uses hot recycled gas as the heat-transport medium (Fig. 6). The unique feature of the UNISHALE processes is the rock pump. The soflds move upward through the retort as the vapors are moving downward. The rock pump was used ia the UNISHALE technology at Parachute, Colorado to produce more than 0.64 x 10 m (four million battels) of cmde shale oil. Operations were shut down in 1991. [Pg.349]

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).
The catalyst is then transferred back to the first process reactor and is reheated to the reforming process temperature at the reactor inlet using a flow of hydrogen-rich process recycle gas, thereby achieving reduction of the platinum to a catalyticaUy active state. [Pg.223]

Oxidation and chlorination of the catalyst are then performed to ensure complete carbon removal, restore the catalyst chloride to its proper level, and maintain full platinum dispersion on the catalyst surface. Typically, the catalyst is oxidized in sufficient oxygen at about 510°C for a period of six hours or more. Sufficient chloride is added, usually as an organic chloride, to restore the chloride content and acid function of the catalyst and to provide redispersion of any platinum agglomeration that may have occurred. The catalyst is then reduced to return the metal components to their active form. This reduction is accompHshed by using a flow of electrolytic hydrogen or recycle gas from another Platforming unit at 400 to 480°C for a period of one to two hours. [Pg.224]

Figure 3 shows a simple schematic diagram of an oxygen-based process. Ethylene, oxygen, and the recycle gas stream are combined before entering the tubular reactors. The basic equipment for the reaction system is identical to that described for the air-based process, with one exception the purge reactor system is absent and a carbon dioxide removal unit is incorporated. The CO2 removal scheme illustrated is based on a patent by Shell Oil Co. (127), and minimises the loss of valuable ethylene in the process. [Pg.458]

Raw Material Purity Requirements. The oxygen process has four main raw materials ethylene, oxygen, organic chloride inhibitor, and cycle diluent. The purity requirements are estabHshed to protect the catalyst from damage due to poisons or thermal mnaway, and to prevent the accumulation of undesirable components in the recycle gas. The latter can lead to increased cycle purging, and consequently higher ethylene losses. [Pg.459]

Ga.s circulation. Recycle gas through heat exchangers to cool or heat. [Pg.1568]

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]

Reformer charge Reformer effluent Hydrocracker charge effluent Recycle gas... [Pg.39]

A large quantity of hydrogen-rich separator gas is normally recycled with the feed stream. Recycle rates may vary from 2,000 to 10,000 MSCF/B. The recycle gas serves to suppress catalyst coke make but normally has relatively little direct effect on gasoline yields or catalyst requirement. However, at lower recycle levels, where an increase in recycle rate may significantly increase reactor hydrogen partial pressure, the effect is similar to a small increase in total... [Pg.51]


See other pages where Recycled gas is mentioned: [Pg.282]    [Pg.844]    [Pg.101]    [Pg.391]    [Pg.427]    [Pg.278]    [Pg.457]    [Pg.351]    [Pg.386]    [Pg.410]    [Pg.224]    [Pg.224]    [Pg.269]    [Pg.277]    [Pg.329]    [Pg.456]    [Pg.457]    [Pg.2371]    [Pg.235]    [Pg.51]    [Pg.53]    [Pg.53]    [Pg.54]    [Pg.54]    [Pg.56]    [Pg.62]    [Pg.98]    [Pg.114]    [Pg.91]    [Pg.91]   
See also in sourсe #XX -- [ Pg.62 ]




SEARCH



Alternatives to gas recycle

Combustion recycled flue gases

Effect of first catalyst exit gas recycle on overall acid plant performance

Effect of gas recycle on first catalyst SO2 oxidation efficiency

Flue gas recycling

Gas recycle

Gas recycle

Gas recycle process

Gas recycling

Gas recycling

Gas recycling calculations

Hot gas recycle process

Hydrogen-to-Oil Ratio and Gas Recycle

Industrial SO3 gas recycle

Outlet gas conditions and recycle of fines

Recycle gas rate

Recycle gas, composition

Recycled flue gases

Single Adiabatic Tubular Reactor Systems with Gas Recycle

© 2024 chempedia.info