Stripping steam

Steam stripping is used to remove dilute concentrations of ammonia, hydrogen sulfide, and other volatile components from pharmaceutical waste stream. Steam stripping can typically achieve contaminant removal of 99% or better and is effective for the removal of organics having boiling points of less than 150 C. The steam stripping process is carried out in a distillation column, which may be either a packed or tray tower. Steam enters at the bottom ofthe column while waste water is countercurrently supplied fi om the top of the distillation column. The product stream, rich in volatile components, may further be treated to recover these components. 

Steam strippers are generally designed by the use of computer simulation programs, although preliminary estimates can be prepared by modifica- 

Although steam stripping is used commercially, it is not without drawbacks. The primary drawback is the additional capital and operational costs to install such a system. In addition, there are other process issues that must also be addressed carefully. 

It is generally not necessary to concentrate the vapors in a reflux condenser and this should be taken into account for added corrosion protection. 

With refluxing, special high cost steel is no guarantee against rapid perforation. It is preferable to utilize a thick Teflon- or friran resin-based coating, a tried and true solution. 

Stripping eliminates 90 to 98% of the sulfides in a wide range of temperatures (75 to 110°) and 92 to 97% of the volatile ammonia but in a higher temperature range and with steam make up. Phenols themselves are stripped fairly little, especially if there is no reflux. 

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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. 

Elimination of unreacted monomers can be accompHshed by two methods dual initiators to enhance conversion of monomers to product (73—75) and steam stripping (70,76). Several process improvements have been claimed for dewatering beads (77), to reduce ha2e (78—81), improve color (82—86), remove monomer (87,88), and maintain homogeneous copolymer compositions (71,72,89). 

Recovery of Ammonia. The filter Hquor contains unreacted sodium chloride and substantially all the ammonia with which the brine was originally saturated. The ammonia may be fixed or free. Fixed ammonia (ammonium chloride [12125-02-97]) corresponds stoichiometrically to the precipitated sodium bicarbonate. Free ammonia includes salts such as ammonium hydroxide, bicarbonate, and carbonate, and the several possible carbon—ammonia compounds that decompose at moderate temperatures. A sulfide solution may be added to the filter Hquor for corrosion protection. The sulfide is distilled for eventual absorption by the brine in the absorber. As the filter Hquor enters the distiller, it is preheated by indirect contact with departing gases. The warmed Hquor enters the main coke, tile, or bubble cap-fiUed sections of the distiller where heat decomposes the free ammonium compounds and steam strips the ammonia and carbon dioxide from the solution. 

Shell process. Universal Oil Pro-ducts sulfolane sulfolane selectivity and capacity insensitive to water content caused by steam-stripping during solvent recov-ery heavy paraffinic countersolvent use 120 rotating-disk contactor, up to 4 m in diameter the high selectivity and capacity of sulfolane leads to low solvent-feed ratios, and thus smaller equip-ment... 

One frozen dessert is made with Simplesse, a protein-based fat mimetic that contains no fat (37). Other dairy product developments include a fat flavor, produced by encapsulating milk fatty acids in maltodextrins (38) fat-free cottage cheeses and 2% fat milk, prepared by steam stripping cream with partial fat addback, with a cholesterol level about 60% lower than the starting material (39). 

Process condensate from reforming operations is commonly treated by steam stripping. More recentiy the stripper has been designed to operate at a... 

Some slurry processes use continuous stirred tank reactors and relatively heavy solvents (57) these ate employed by such companies as Hoechst, Montedison, Mitsubishi, Dow, and Nissan. In the Hoechst process (Eig. 4), hexane is used as the diluent. Reactors usually operate at 80—90°C and a total pressure of 1—3 MPa (10—30 psi). The solvent, ethylene, catalyst components, and hydrogen are all continuously fed into the reactor. The residence time of catalyst particles in the reactor is two to three hours. The polymer slurry may be transferred into a smaller reactor for post-polymerization. In most cases, molecular weight of polymer is controlled by the addition of hydrogen to both reactors. After the slurry exits the second reactor, the total charge is separated by a centrifuge into a Hquid stream and soHd polymer. The solvent is then steam-stripped from wet polymer, purified, and returned to the main reactor the wet polymer is dried and pelletized. Variations of this process are widely used throughout the world. 

The reaction is completed after 6—8 h at 95°C volatiles, water, and some free phenol are removed by vacuum stripping up to 140—170°C. For resins requiring phenol in only trace amounts, such as epoxy hardeners, steam distillation or steam stripping may be used. Both water and free phenol affect the cure and final resin properties, which are monitored in routine quaHty control testing by gc. OxaHc acid (1—2 parts per 100 parts phenol) does not require neutralization because it decomposes to CO, CO2, and water furthermore, it produces milder reactions and low color. Sulfuric and sulfonic acids are strong catalysts and require neutralization with lime 0.1 parts of sulfuric acid per 100 parts of phenol are used. A continuous process for novolak resin production has been described (31,32). An alternative process for making novolaks without acid catalysis has also been reported (33), which uses a... 

Process condensate from reforming operations is commonly treated by steam stripping. The stripper is operated at a sufficiently high pressure to allow the overhead stripping steam to be used as part of the reformer steam requirement (71). Contaminants removed from the process condensate are reformed to extinction, so disposal to the environment is thereby avoided. This system not only reduces atmospheric emissions, but contributes to the overall efficiency of the process by recovering condensate suitable for boiler feedwater make-up because the process is a net water consumer. 

The Hquor is then treated with calcium hydroxide (milk of lime) which reacts with the fixed salts, mosdy ammonium chloride, to Hberate ammonia. The Hquor is regenerated in a steam stripping operation. 

One of the key benefits of anionic PS is that it contains much lower levels of residual styrene monomer than free-radical PS (167). This is because free-radical polymerization processes only operate at 60—80% styrene conversion, whereas anionic processes operate at >99% styrene conversion. Removal of unreacted styrene monomer from free-radical PS is accompHshed using continuous devolatilization at high temperature (220—260°C) and vacuum. This process leaves about 200—800 ppm of styrene monomer in the product. Taking the styrene to a lower level requires special devolatilization procedures such as steam stripping (168). 

Process water streams from vinyl chloride manufacture are typically steam-stripped to remove volatile organics, neutralized, and then treated in an activated sludge system to remove any nonvolatile organics. If fluidized-bed oxychlorination is used, the process wastewater may also contain suspended catalyst fines and dissolved metals. The former can easily be removed by sedimentation, and the latter by precipitation. Depending on the specific catalyst formulation and outfall limitations, tertiary treatment may be needed to reduce dissolved metals to acceptable levels. 

Kinetics of suspension PVC are identical to the kinetics of mass PVC, both increasing in rate with conversion (90). After polymerization to about 80—90% conversion, excess monomer is recovered, the slurry is steam-stripped in a column to a residual monomer level of about 0.0001% (10 ppm), excess water is centrifuged off, and the resin is dried with hot air. 

After mixing, the solvent and waste are separated. The solvent with dissolved organics is called the extract. The waste remaining after extraction is called the raffinate. The extract may be sent to a distillation or steam stripping unit to separate the dissolved organics from the solvent and the solvent can be recycled back to the extraction process. The raffinate may require additional treatment or may be disposed or incinerated. 

Chemical precipitation Chemical oxidation/re duction Air and/or steam stripping Activated carbon adsorption Resin adsorption Ion exchange Ultrafiltra-tion and/or reverse osmosis Flo atation / ph ase separation... 

The refining process most commonly used involves treatment with hot aqueous alkaH to convert free fatty acids to soaps, followed by bleaching, usually with hydrogen peroxide, although sodium chlorite, sodium hypochlorite, and ozone have also been used. Other techniques include distillation, steam stripping, neutralization by alkaH, Hquid thermal diffusion, and the use of active adsorbents, eg, charcoal and bentonite, and solvent fractionation... 

There are two commercial solvent crystaUi2ation processes. The Emersol Process, patented in 1942 by Emery Industries, uses methanol as solvent and the Armour-Texaco Process, patented in 1948, uses acetone as solvent. The fatty acids to be separated are dissolved in the solvent and cooled, usually in a double-pipe chiller. Internal scrapers rotating at low rpm remove the crystals from the chilled surface. The slurry is then separated by means of a rotary vacuum filter. The filter cake is sprayed with cold solvent to remove free Hquid acids, and the solvents are removed by flash evaporation and steam stripping and recovered for reuse (10). 

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