Hydrocarbon stripping

Cj—C(j hydrocarbons Stripped from water with helium Helium stripped hydrocarbons can be adsorbed on to carbon to increase sensitivity [Pg.325]

Constant in Strigle s HETP equation for hydrocarbon stripping, Eq. (9.37)... 

Rich solvent from the bottom of the EDC is routed to the solvent-recovery column (SRC), where the aromatics are stripped overhead. Stripping steam from a closed-loop water circuit facilitates hydrocarbon stripping. The SRC operates under vacuum to reduce the boiling point at the column base. 

Dandekar, A.B., et al. Regeneration of Aromatic Alkylation Catalysts Using Hydrocarbon Stripping. WO 01/83408, Nov 2001. Mobil Oil Corp, Baytown, TX. 

Figure 23,2.6. GCW process diagram. Effective hydrocarbon stripping in the water column is observed in these systems using a vacuum extraction. A circulation cell is created by directional flow of water in the vertieal direetion creating a capture zone extending several meters from the well. In addition a bioreactor (high surface area baeteiial biofilm) can be used in the system to degrade low volatile contaminants [Adapted from Bemhartt et al., U.S. Patent 5,910,245,1999]...

The hydrocarbons stripped off the catalyst are returned to the reactor and eventually recovered as products. The hydrocarbons left on the catalyst are burned in the regenerator with the following debits ... 

Ci-Ct hydrocarbons Stripped from water with helium - -... 

The solubility of hydrocarbon liquids from the same chemical family diminishes as the molecular weight increases. This effect is particularly sensitive thus in the paraffin series, the solubility expressed in mole fraction is divided by a factor of about five when the number of carbon atoms is increased by one. The result is that heavy paraffin solubilities are extremely small. The polynuclear aromatics have high solubilities in water which makes it difficult to eliminate them by steam stripping. 

A general, approximate, short-cut design procedure for adiabatic bubble tray absorbers has not been developed, although work has been done in the field of nonisothermal and multicomponent hydrocarbon absorbers. An analytical expression which will predict the recovery of each component provided the stripping factor, ie, the group is known for each component on each tray of the column has been developed (102). This requires knowledge... 

Butadiene Separation. Solvent extraction is used in the separation of butadiene (qv) [106-99-0] from other C-4 hydrocarbons in the manufacture of synthetic mbber. The butadiene is produced by catalytic dehydrogenation of butylene and the Hquid product is then extracted using an aqueous cuprammonium acetate solution with which the butadiene reacts to form a complex. Butadiene is then recovered by stripping from the extract. Distillation is a competing process. 

Polymerizations are typically quenched with water, alcohol, or base. The resulting polymerizates are then distilled and steam and/or vacuum stripped to yield hard resin. Hydrocarbon resins may also be precipitated by the addition of the quenched reaction mixture to an excess of an appropriate poor solvent. As an example, aUphatic C-5 resins are readily precipitated in acetone, while a more polar solvent such as methanol is better suited for aromatic C-9 resins. 

Condensable hydrocarbons are removed from natural gas by cooling the gas to a low temperature and then by washing it with a cold hydrocarbon hquid to absorb the condensables. The uncondensed gas (mainly methane with a small amount of ethane) is classified as natural gas. The condensable hydrocarbons (ethane and heavier hydrocarbons) are stripped from the solvent and are separated into two streams. The heavier stream, which largely contains propane with some ethane and butane, can be Hquefied and is marketed as Hquefied petroleum gas (LPG) (qv). The heavier fractions, which consist of and heavier hydrocarbons, are added to gasoline to control volatihty (see Gasoline and other motor fuels). 

Naphtha desulfurization is conducted in the vapor phase as described for natural gas. Raw naphtha is preheated and vaporized in a separate furnace. If the sulfur content of the naphtha is very high, after Co—Mo hydrotreating, the naphtha is condensed, H2S is stripped out, and the residual H2S is adsorbed on ZnO. The primary reformer operates at conditions similar to those used with natural gas feed. The nickel catalyst, however, requires a promoter such as potassium in order to avoid carbon deposition at the practical levels of steam-to-carbon ratios of 3.5—5.0. Deposition of carbon from hydrocarbons cracking on the particles of the catalyst reduces the activity of the catalyst for the reforming and results in local uneven heating of the reformer tubes because the firing heat is not removed by the reforming reaction. 

Polymerization in Solution or Slurry. Many hydrocarbon solvents dissolve PE at elevated temperatures of 120—150°C. Polymerization reactions in solution requite, as theit last step, the stripping of solvent. A variety of catalysts can be used in these processes. 

In general, the sulfolane extraction unit consists of four basic parts extractor, extractive stripper, extract recovery column, and water—wash tower. The hydrocarbon feed is first contacted with sulfolane in the extractor, where the aromatics and some light nonaromatics dissolve in the sulfolane. The rich solvent then passes to the extractive stripper where the light nonaromatics are stripped. The bottom stream, which consists of sulfolane and aromatic components, and which at this point is essentiaHy free of nonaromatics, enters the recovery column where the aromatics are removed. The sulfolane is returned to the extractor. The non aromatic raffinate obtained initially from the extractor is contacted with water in the wash tower to remove dissolved sulfolane, which is subsequently recovered in the extract recovery column. Benzene and toluene recoveries in the process are routinely greater than 99%, and xylene recoveries exceed 95%. 

The energy requirements for desorbing 1,1-dichloroethane from activated carbon in a stripping—adsorption process for water purification have been calculated at 112 kj/kg (14). Chlorinated hydrocarbons such as 1,1-dichloroethane may easily be removed from water by air or steam stripping. 

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