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Residual gas

In molecular distillation, the permanent gas pressure is so low (less than 0 001 mm. of mercury) that it has very little influence upon the speed of the distillation. The distillation velocity at such low pressures is determined by the speed at which the vapour from the liquid being distilled can flow through the enclosed space connecting the still and condenser under the driving force of its own saturation pressure. If the distance from the surface of the evaporating liquid to the condenser is less than (or of the order of) the mean free path of a molecule of distillate vapour in the residual gas at the same density and pressure, most of the molecules which leave the surface will not return. The mean free path of air at various pressures is as follows —... [Pg.120]

Residential sheathing Residual fuel Residual fuel oil Residual gas analyzers... [Pg.848]

Any hydrogen contained within the chlorine from the electroly2er is concentrated in the residual gas from the Hquefaction process and must not be allowed to exceed the explosive concentration limit of 5%. Although hydrogen concentration can be controUed by adding dry air to the process. [Pg.502]

Fig. 35. Explosive limits of CI2—H2—other gas mixtures where M represents the explosive region in the presence of residue gas from CI2 Hquefaction (O2,... Fig. 35. Explosive limits of CI2—H2—other gas mixtures where M represents the explosive region in the presence of residue gas from CI2 Hquefaction (O2,...
Flame or Partial Combustion Processes. In the combustion or flame processes, the necessary energy is imparted to the feedstock by the partial combustion of the hydrocarbon feed (one-stage process), or by the combustion of residual gas, or any other suitable fuel, and subsequent injection of the cracking stock into the hot combustion gases (two-stage process). A detailed discussion of the kinetics for the pyrolysis of methane for the production of acetylene by partial oxidation, and some conclusions as to reaction mechanism have been given (12). [Pg.386]

Dry inlet gas that has been dehydrated by molecular sieves (qv) or alumina beds to less than 0.1 ppm water is spHt into two streams by a three-way control valve. Approximately 60% of the inlet gas is cooled by heat exchange with the low pressure residue gas from the demethanizer and by external refrigeration. The remainder of the inlet gas is cooled by heat exchange with the demethanized bottoms product, the reboiler, and the side heater. A significant amount of low level refrigera tion from the demethanizer Hquids and the cold residue gas stream is recovered in the inlet gas stream. [Pg.182]

Essentially all of the methane [74-82-8] is removed ia the demethanizer overhead gas product. High recovery of ethane and heavier components as demethanizer bottoms products is commonplace. The work that is generated by expanding the gas ia the turboexpander is utilized to compress the residue gas from the demethanizer after it is warmed by heat exchange with the inlet gas. Recompression and deUvery to a natural gas pipeline is performed downstream of the plant. A propane recovery of 99% can be expected when ethane recoveries are ia excess of 65%. [Pg.183]

The rich oil from the absorber is expanded through a hydrauHc turbiae for power recovery. The fluid from the turbiae is flashed ia the rich-oil flash tank to 2.1 MPa (300 psi) and —32°C. The flash vapor is compressed until it equals the inlet pressure before it is recycled to the inlet. The oil phase from the flash passes through another heat exchanger and to the rich-oil deethanizer. The ethane-rich overhead gas produced from the deethanizer is compressed and used for produciag petrochemicals or is added to the residue-gas stream. [Pg.183]

Sulfur Compounds. Various gas streams are treated by molecular sieves to remove sulfur contaminants. In the desulfurization of wellhead natural gas, the unit is designed to remove sulfur compounds selectively, but not carbon dioxide, which would occur in Hquid scmbbing processes. Molecular sieve treatment offers advantages over Hquid scmbbing processes in reduced equipment size because the acid gas load is smaller in production economics because there is no gas shrinkage (leaving CO2 in the residue gas) and in the fact that the gas is also fliUy dehydrated, alleviating the need for downstream dehydration. [Pg.456]

The need to obtain greater recoveries of the C9, C3, and C4S in natural gas has resulted in the expanded use of low-temperature processing of these streams. The majority of the natural gas processing at low temperatures to recover light hydrocarbons is now accomphshed using the turboexpander cycle. Feed gas is normally available from 1 to 10 MPa. The gas is first dehydrated to a dew point of 200 K and lower. After dehydration the feed is cooled with cold residue gas. Liquid produced at this point is separated before entering the expander and sent to the condensate stabilizer. The gas from the separator is... [Pg.1133]

Vacuum Insulation Heat transport across an evacuated space (1.3 X lO"" Pa or lower), is by radiation and by conduction through the residual gas. The heat transfer by radiation generally is predominant and can be approximated by... [Pg.1134]

FIG. 22-77 Influence of feed purity on total membrane area when the residue gas at fixed purity is the product, Feed-gas volume is constant, CO2/CH4 cellulose-acetate membrane, (X = 21, Courtesy VP R. Grace.)... [Pg.2052]

Figure 2-5 shows another applieation for turboexpanders, one that requires -100 or -150°F for the separation of propane and heavier hydroearbons from a natural gas stream. The produet is almost always reeovered as a liquid, whieh introduees a large additional refrigeration load. The residue gas diseharge pressure usually must be maintained as high as possible, so effieieney is important. [Pg.24]

LNG—consisting of ethane, propane, butane, and natural gasoline (condensate)—arrives at the plant for upgrading before it is sent to petrochemical plants and refineries as feedstock. Residue gas is sold to the interstate and intrastate pipeline network. MESA, one of the world s major crude helium producers, also delivers helium to a pipeline operated by the U.S. Bureau of Mines. [Pg.449]

Gas emerges from each expander cooled to -61°C (-77°F). Additional heat exchangers lower the temperature to -84°C (-120°F), at which point all the LNG is removed for delivery. Residue gas, now under reduced pressure, is passed along to the nitrogen rejection unit (NRU) where inert nitrogen is separated and vented into the atmosphere. Helium is also recovered in the NRU. The remaining residue gas is 90% methane. [Pg.450]

Next, the upgraded residue gas is raised back to 34 bar (500 psig) for delivery to customers. The gas stream is introduced into the compressor end, where it is boosted from 8 to 10 bar (120 to 145 psig). The stream continues to the second compressor, where pressure is raised to 12 bar (170 psig). [Pg.450]

The basic principle of e-beam SNMS as introduced by Lipinsky et al. in 1985 [3.60] is simple (Fig. 3.30) - as in SIMS, the sample is sputtered with a focused keV ion beam. SN post-ionization is accomplished by use of an e-beam accelerated between a filament and an anode. The applied electron energy Fe a 50 20 eV is higher than the range of first ionization potentials (IP) of the elements (4—24 eV, see Fig. 3.31). Typical probabilities of ionization are in the 0.01% range. SD and residual gas suppression is achieved with electrostatic lenses before SN post-ionization and energy filtering, respectively. [Pg.123]

For IBSCA analysis, standard HV or, better, UHV-equipment with turbomolecular pump and a residual gas pressure of less than 10 Pa is necessary. As is apparent from Fig. 4.46, the optical detection system, which consists of transfer optics, a spectrometer, and a lateral-sensitive detector, is often combined with a quadrupole mass spectrometer for analysis of secondary sputtered particles (ions or post-ionized neutrals). [Pg.242]

For intermediate temperatures from 400-1000°C (Fig. 11), the volatilization of carbon atoms by energetic plasma ions becomes important. As seen in the upper curve of Fig. 11, helium does not have a chemical erosion component of its sputter yield. In currently operating machines the two major contributors to chemical erosion are the ions of hydrogen and oxygen. The typical chemical species which evolve from the surface, as measured by residual gas analysis [37] and optical emission [38], are hydrocarbons, carbon monoxide, and carbon dioxide. [Pg.414]

The gas is routed through heat exchangers where it is cooled by the residue gas, and condensed liquids are recovered in a cold separator at appro.ximately -90°F. These liquids are injected into the de-methanizer at a level where the temperature is approximately -90°F. The gas is (hen expanded (its pressure is decreased from inlet pressure to 22.3 psig) through an expansion valve or a turboexpander. The turboexpander Lises the energy removed from the gas due to the pressure drop to drive a compressor, which helps recompress the gas to sales pressure. The cold gas f-)50°F) then enters the de-methanizer column at a pressure and temperature condition where most of the ethanes-plus Lire in the liquid state. [Pg.248]

The de-methanizer is analogous to a cold feed condensate stabilizer As the liquid falls and is heated, the methane is boiled off and the liquid becomes leaner and leaner in methane. Heat is added to the bottom of the tower using the hot discharge residue gas from the compressors to assure that the bottom liquids have an acceptable RVP or methane content. [Pg.249]

Propane cracking is similar to ethane except for the furnace temperature, which is relatively lower (longer chain hydrocarbons crack easier). However, more by-products are formed than with ethane, and the separation section is more complex. Propane gives lower ethylene yield, higher propylene and butadiene yields, and significantly more aromatic pyrolysis gasoline. Residual gas (mainly H2 and methane) is about two and half times that produced when ethane is used. Increasing the severity... [Pg.97]

Figure 8-4. A flow diagram for the hydration of propylene to isopropanol (1) propylene recovery column, (2) reactor, (3) residual gas separation column, (4) aqueous - isopropanol azeotropic distillation column, (5) drying column, (6) isopropyl ether separator, (7) isopropyl ether extraction. Figure 8-4. A flow diagram for the hydration of propylene to isopropanol (1) propylene recovery column, (2) reactor, (3) residual gas separation column, (4) aqueous - isopropanol azeotropic distillation column, (5) drying column, (6) isopropyl ether separator, (7) isopropyl ether extraction.

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