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Using Sweep Gases

If the oxygen partial pressure on the two sides of an OTM is different, according to eqns (16.3) and (16.4), an oxygen flux starts to compensate this [Pg.196]


Another measure to increase the hydrogen partial pressure difference between permeate and retenate is to use sweep gas on the retenate side. Because the hydrogen requires humidification for low temperature PEM fuel cells to prevent membrane dry-out, steam is the preferred sweep gas [405]. OHany et al. highlighted the effect of steam as the sweep gas for the permeate in a methane steam reforming membrane reactor [406]. Higher methane conversion was observed, which originated from back-diffusion of steam from the permeate to the reaction side of the membrane, which increased the S/C ratio and consequently the conversion. [Pg.166]

Khayet, M., Godino, P., and Mengual, J. I. (2003a). Theoretical and experimental studies on desalination using sweeping gas membrane method. Desalination 157, 297. [Pg.365]

Depending on the type of nebulizer used and its efficiency, there may be initially a significant proportion of large droplets in the aerosol. Heavier than the very fine droplets, the larger droplets are affected by gravity and by turbulent flow in the argon sweep gas, which cause them to deposit onto the walls of the transfer tube. [Pg.400]

Nitrogen is used for pressure maintenance in oil and gas reservoirs for enhanced recovery. It is sometimes used as a miscible agent to reduce oil viscosity and increase recovery in deep reservoirs. Other appHcations include recovery of oil in attic formations, gas cap displacement, and a sweep gas for miscible CO2 slugs. Nitrogen competes with CO2, a more miscible gas with hydrocarbons (qv), in most of these appHcations. The production mode is typically by on-site cryogenic separation plants. In 1990, nitrogen production in enhanced recovery operations was 20 x 10 m /d (750 million SCF/d)... [Pg.80]

DP systems can be shut down when not in use to conserve energy. If a Hquid-nitrogen trap is incorporated, the manner in which this trap is warmed up and the DP is cooled down should be deterniined by the presence or absence of a valve between the chamber and the Hquid-nitrogen trap. In critical systems, this head valve can be included in order to permit rapid shutdown and rapid return to operation. The assertion that dry nitrogen gas can be used to sweep contamination from traps and pumps in such manner that oil contamination is prevented from mnning counter to the nitrogen-sweeping flow direction is questionable. Proper placement of valves can eliminate the need of a sweep gas. [Pg.378]

Water Transport. Two methods of measuring water-vapor transmission rates (WVTR) ate commonly used. The newer method uses a Permatran-W (Modem Controls, Inc.). In this method a film sample is clamped over a saturated salt solution, which generates the desired humidity. Dry air sweeps past the other side of the film and past an infrared detector, which measures the water concentration in the gas. For a caUbrated flow rate of air, the rate of water addition can be calculated from the observed concentration in the sweep gas. From the steady-state rate, the WVTR can be calculated. In principle, the diffusion coefficient could be deterrnined by the method outlined in the previous section. However, only the steady-state region of the response is serviceable. Many different salt solutions can be used to make measurements at selected humidity differences however, in practice,... [Pg.500]

Process development on fluidized-bed pyrolysis was also carried out by the ConsoHdation Coal Co., culminating in operation of a 32 t/d pilot plant (35). The CONSOL pyrolysis process incorporated a novel stirred carbonizer as the pyrolysis reactor, which made operation of the system feasible even using strongly agglomerating eastern U.S. biturninous coals. This allowed the process to bypass the normal pre-oxidation step that is often used with caking coals, and resulted in a nearly 50% increase in tar yield. Use of a sweep gas to rapidly remove volatiles from the pyrolysis reactor gave overall tar yields of nearly 25% for a coal that had Eischer assay tar yields of only 15%. [Pg.287]

As an example the use of ceramic membranes for ethane dehydrogenation has been discussed (91). The constmction of a commercial reactor, however, is difficult, and a sweep gas is requited to shift the product composition away from equiUbrium values. The achievable conversion also depends on the permeabihty of the membrane. Figure 7 shows the equiUbrium conversion and the conversion that can be obtained from a membrane reactor by selectively removing 80% of the hydrogen produced. Another way to use membranes is only for separation and not for reaction. In this method, a conventional, multiple, fixed-bed catalytic reactor is used for the dehydrogenation. After each bed, the hydrogen is partially separated using membranes to shift the equihbrium. Since separation is independent of reaction, reaction temperature can be optimized for superior performance. Both concepts have been proven in bench-scale units, but are yet to be demonstrated in commercial reactors. [Pg.443]

Vapors (from drying) are removed at the feed end of the dtyer to the atmosphere through a natural-draft stack and settling chamber or wet scrubber. When employed in simple drying operations with 3.5 X 10 to 10 X 10 Pa steam, draft is controlled by a damper to admit only sufficient outside air to sweep moisture from the cylinder, discharging the air at 340 to 365 K and 80 to 90 percent saturation. In this way, shell gas velocities and dusting are minimized. When used for solvent recovery or other processes requiring a sealed system, sweep gas is recirculated throu a scrubber-gas cooler and blower. [Pg.1209]

Transport properties have been studied before and after Si deposition using a rig similar to the one for catalytic testings (Figure 2). Pure gas permeabilities (H2, He, N2, normal and isobutane) were studied by measuring the flux passing though the membrane as a function of temperature and pressure for a constant transmembrane differential pressure (no sweep gas). [Pg.128]

Gas separation performances (H2/n-butane, n-hexane/2-2 dimethylbutane) have been measured using a sweep gas (countercurrent mode) in order to increase the permeation driving force (no differential pressure was used) permeate and retentate compositions (see Figure 2) were analysed using on line gas chromatography. [Pg.129]

Catalytic testings have been performed using the same rig and a conventional fixed-bed placed in the inner volume of the tubular membrane. The catalyst for isobutane dehydrogenation [9] was a Pt-based solid and sweep gas was used as indicated in Fig. 2. For propane oxidative dehydrogenation a V-Mg-0 mixed oxide [10] was used and the membrane separates oxygen and propane (the hydrocarbon being introduced in the inner part of the reactor). [Pg.129]

Membrane System Design Features For the rate process of permeation to occur, there must be a driving force. For gas separations, that force is partial pressure (or fugacity). Since the ratio of the component fluxes determines the separation, the partial pressure of each component at each point is important. There are three ways of driving the process Either high partial pressure on the feed side (achieved by high total pressure), or low partial pressure on the permeate side, which may be achieved either by vacuum or by introduction of a sweep gas. Both of the permeate options have negative economic impHcations, and they are less commonly used. [Pg.60]

In the discussion of concentration polarization to this point, the assumption is made that the volume flux through the membrane is large, so the concentration on the permeate side of the membrane is determined by the ratio of the component fluxes. This assumption is almost always true for liquid separation processes, such as ultrafiltration or reverse osmosis, but must be modified in a few gas separation and pervaporation processes. In these processes, a lateral flow of gas is sometimes used to change the composition of the gas on the permeate side of the membrane. Figure 4.14 illustrates a laboratory gas permeation experiment using this effect. As the pressurized feed gas mixture is passed over the membrane surface, certain components permeate the membrane. On the permeate side of the membrane, a lateral flow of helium or other inert gas sweeps the permeate from the membrane surface. In the absence of the sweep gas, the composition of the gas mixture on the permeate side of the membrane is determined by the flow of components from the feed. If a large flow of sweep gas is used, the partial... [Pg.182]

Figure 4.14 (a) Flow schematic of permeation using a permeate-side sweep gas sometimes used in laboratory gas separation and pervaporation experiments, (b) The concentration gradients that form on the permeate side of the membrane depend on the volume of sweep gas used. In laboratory experiments a large sweep-gas-to-permeate-gas flow ratio is used, so the concentration of permeate at the membrane surface is very low... [Pg.182]

The drawback of using an external permeate-side sweep gas to lower the partial pressure on the permeate side of the membrane for an industrial process is that the sweep gas and permeating component must subsequently be separated. In some cases this may not be difficult some processes that have been suggested but rarely used are shown in Figure 4.15. In these examples, the separation of the sweep gas and the permeating component is achieved by condensation. If the permeating gas is itself easily condensed, an inert gas such as nitrogen can be used as the sweep [18], An alternative is a condensable vapor such as steam [19-21],... [Pg.183]

In the case of the counter-flow/sweep membrane module illustrated in Figure 4.18(c) a portion of the dried residue gas stream is expanded across a valve and used as the permeate-side sweep gas. The separation obtained depends on how much gas is used as a sweep. In the calculation illustrated, 5 % of the residue gas is used as a sweep even so the result is dramatic. The concentration of water vapor in the permeate gas is 13 000 ppm, almost the same as the perfect counter-flow module shown in Figure 4.18(b), but the membrane area required to perform the separation is one-third of the counter-flow case. Mixing separated residue gas with the permeate gas improves the separation The cause of this paradoxical result is illustrated in Figure 4.19 and discussed in a number of papers by Cussler et al. [16]. [Pg.187]

An alternative carrier-gas system uses a condensable gas, such as steam, as the carrier sweep fluid. One variant of this system is illustrated in Figure 9.7(d). Low-grade steam is often available at low cost, and, if the permeate is immiscible with the condensed carrier, water, it can be recovered by decantation. The condensed water will contain some dissolved organic and can be recycled to the evaporator and then to the permeate side of the module. This operating mode is limited to water-immiscible permeates and to feed streams for which contamination of the feed liquid by water vapor permeating from the sweep gas is not a problem. This idea has been discovered, rediscovered, and patented a number of times, but never used commercially [37,38], If the permeate is soluble in the condensable... [Pg.369]

Sweeping-gas membrane distillation (SGMD), in which a stripping gas, instead of vacuum, is used as a carrier... [Pg.291]

Pervaporation is a concentration-driven membrane process for liquid feeds. It is based on selective sorption of feed compounds into the membrane phase, as a result of differences in membrane-solvent compatibility, often referred to as solubility in the membrane matrix. The concentration difference (or, in fact, the difference in chemical potential) is obtained by applying a vacuum at the permeate side, so that transport through the membrane matrix occurs by diffusion in a transition from liquid to vapor conditions (Figure 3.1). Alternatively, a sweep gas can be used to obtain low vapor pressures at the permeate side with the same effect of a chemical potential gradient. [Pg.46]

In the case of the counterflow/sweep membrane module illustrated in Figure 8.5 (c), a portion of the dried residue gas stream is expanded across a valve and used as the permeate-side sweep gas. The separation obtained depends on how much gas is used... [Pg.174]


See other pages where Using Sweep Gases is mentioned: [Pg.25]    [Pg.196]    [Pg.196]    [Pg.434]    [Pg.263]    [Pg.186]    [Pg.332]    [Pg.2050]    [Pg.47]    [Pg.307]    [Pg.87]    [Pg.102]    [Pg.137]    [Pg.100]    [Pg.131]    [Pg.531]    [Pg.160]    [Pg.212]    [Pg.182]    [Pg.228]    [Pg.61]    [Pg.13]    [Pg.183]    [Pg.183]    [Pg.348]    [Pg.371]    [Pg.449]    [Pg.500]    [Pg.503]    [Pg.355]    [Pg.201]    [Pg.288]   


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Gases using

SWEEP-GAS

Sweep

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