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Vacuum distillation systems system

The ice bath is removed after addition of the sodium cyanide, and the mixture is stirred for 4 hours. The organic layer is separated, and the aqueous layer is extracted with three 500-ml. portions of ether. The combined ethereal extracts and organic layer are washed with two 100-ml. portions of cold water and dried over anhydrous magnesium sulfate. The ethereal solution is filtered, and the ether is removed at atmospheric pressure. The residue is transferred to a vacuum distillation system and distilled under reduced pressure (Cauiionl See Note 2). The yield of dlmethylaminophenylacetonitrile boiling at 88-90°/l.9-2.1 tnm. is 842 844 g. (87-88%) (Notes 3 and 4). [Pg.25]

The target for americium concentration in the plutonium is <1000 ppm. This means that a 100-fold reduction of americium concentration is necessary. The vacuum distillation system discussed above seems a likely candidate for this step. [Pg.421]

Pressure drop. Packed towers are designed so that the pressure drop at any point in the tower does not exceed a recommended maximum value. Maximum pressure drop criteria for packed towers are listed in Table 8.4. For vacuum distillation, foaming systems, and where fan horsepower needs to be minimized, the pressure drop criteria frequently set tower diameter. [Pg.508]

The crude PA is thermally pretreated (7) and then fed to the vacuum distillation system. Low boiling (LB) impurities are removed in the lights column (8) as LB residues. The high-boiling (HB) residue from the pure PA column (9) is sent to the residue boil-out vessel for PA recovery. Pure PA obtained as a distillate can be stored either in the molten state or flaked and bagged. [Pg.142]

The vacuum-distillation system is improved by distilling with live steam the final 10 per cent of aniline. Such a practice does not introduce a large quantity of water into the system and saves considerable time. The vacuum-distillation system apparently doubles the productivity of the reducers but since the cost of the stills is considerable, the saving is more apparent than real. [Pg.156]

The innovative process using liquid SO2 and liquid SO3 avoids elaborate chain of glasslined reactors with thermic fluid heating and vacuum distillation batch systems in Fig. 8.2. [Pg.54]

Figure 8.2 Vacuum distillation system with a helium counter-flow leak detector connected. Figure 8.2 Vacuum distillation system with a helium counter-flow leak detector connected.
At ordinary temperatures, the equilibrium favors the concentration of deuterium in the water, but at a temperature of around 130 C the equilibrium favors the concentration of deuterium in the hydrogen sulfide. The tower is therefore divided into two sections, the upper or cold section increasing the concentration of deuterium in the water, which is then used as feed for the lower or hot section, where the exchange leads to a further enrichment, this time in the hydrogen sulfide stream. The enriched gas from this section is then led to the second stage for further concentration. In a final stage, deuterium from the enriched gas is transferred to water, which is then fed to a vacuum distillation system for final enrichment to almost pure D2O (99.75%). [Pg.172]

At high temperatures, active sulfur can directly react with metals at any locations in contact with processing media. This sulfidation attack is a kind of uniform corrosion process. H2S is the most corrosive compound in these sulfides. The typical corrosive environments are located at the bottom of the towers of the atmospheric and vacuum distillation systems, pipelines, atmospheric heavy oil heat exchangers and vacuum residuum heat exchangers, the bottom of the main fractionating columns of catalytic cracking equipment and the coke retarding equipment. [Pg.499]

Heavy crude oils with low sulfur and high TAN were processed within the atmospheric and vacuum units in Refinery B. The average TAN was about 3.0 mg KOH/g and the sulfur content was lower than 0.5%. It was found that severe corrosion occurred in the vacuum distillation systems during the inspection carried out in May 2006. The materials used to fabricate the wall of the third and fourth floors of the tower were carbon steel and 316L stainless steel. The inspection revealed that a lot of pits were formed on the inner wall as shown in Fig. 17.3. [Pg.507]

All the packing materials on the second, third and fourth floors of the vacuum distillation system should be upgraded to 316LSS. The oil collection tank on the third floor should be changed. The load and the velocity of flow must be decreased by process control to decrease the corrosion rate. [Pg.511]

In 1840 a hydrauHc power network, which involved large reciprocating pumps that were driven by steam engines, suppHed fluid power to London. However, concurrent technology in steam (qv) turbines and the electric generators outmoded such networks until hydrauHc systems were improved with the use of rotary pumps and oil. The rotary piston pump marked the transition from use of water to oil as the hydrauHc fluid (4). The use of vacuum-distilled, refined mineral oils were instmmental in the success of rotary axial piston pumps and motors such as the Waterbury variable speed gear... [Pg.261]

The design of these distillation systems and the operating conditions used depend on the physical properties of the alkylphenols involved and on the product requirements. Essentially all alkylphenol distillation systems operate under vacuum, but the actual pressures maintained vary considerably. Vacuum operation allows reasonable reboder temperatures (200—350°C) so that thermal dealkylation reactions of the alkylphenols are slow. [Pg.64]

Dialkylphenols are also produced in specialized plants. These plants combine complex batch reactors with vacuum distillation trains or other recovery systems. Alkenes with carbon numbers between 4 and 9 react with phenol to make an unrefined alkylphenol mixture, which is fed into the recovery section where very high purity product is isolated. The product is stored, handled, and shipped just as are the monoalkylphenols. [Pg.64]

The fatty acids that emerge from the top of the column contain entrained water, partially hydroly2ed fat, and the Zn—soap catalyst. This product stream is passed into a vacuum dryer stage where the water is removed through vapori2ation and the fatty acid cooled as a result of this vapori2ation process. The dried product stream is then passed to a distillation system. [Pg.155]

Heat Sensitivity. The heat sensitivity or polymerization tendencies of the materials being distilled influence the economics of distillation. Many materials caimot be distilled at their atmospheric boiling points because of high thermal degradation, polymerization, or other unfavorable reaction effects that are functions of temperature. These systems are distilled under vacuum in order to lower operating temperatures. For such systems, the pressure drop per theoretical stage is frequently the controlling factor in contactor selection. An exceUent discussion of equipment requirements and characteristics of vacuum distillation may be found in Reference 90. [Pg.175]

Heavy water [11105-15-0] 1 2 produced by a combination of electrolysis and catalytic exchange reactions. Some nuclear reactors (qv) require heavy water as a moderator of neutrons. Plants for the production of heavy water were built by the U.S. government during World War II. These plants, located at Trad, British Columbia, Morgantown, West Virginia, and Savaimah River, South Carolina, have been shut down except for a portion of the Savaimah River plant, which produces heavy water by a three-stage process (see Deuterium and tritium) an H2S/H2O exchange process produces 15% D2O a vacuum distillation increases the concentration to 90% D2O an electrolysis system produces 99.75% D2O (58). [Pg.78]

After deactivation and removal of the initiating system, the eoumarone-indene resin is separated from solvent and low moleeular weight materials by vacuum distillation. The removal of the low moleeular weight materials is important beeause they produce strong odour, they aet as softeners and they eause an undesirable deerease in softening point. Therefore, at this stage the softening point of the eoumarone-indene resins is adjusted. Finally, stabilizers are added to the liquid resin while it is still hot to inhibit further oxidation (whieh eauses diseolouration and odour). [Pg.605]


See other pages where Vacuum distillation systems system is mentioned: [Pg.469]    [Pg.170]    [Pg.54]    [Pg.162]    [Pg.106]    [Pg.162]    [Pg.146]    [Pg.146]    [Pg.777]    [Pg.6679]    [Pg.47]    [Pg.510]    [Pg.511]    [Pg.516]    [Pg.516]    [Pg.509]    [Pg.530]    [Pg.89]    [Pg.282]    [Pg.484]    [Pg.198]    [Pg.155]    [Pg.344]    [Pg.11]    [Pg.74]    [Pg.1292]   


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