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Solution multistage

If system forms soHd solution, multistage crystallisation requited (likely to be expensive). [Pg.452]

Solution Filtration. The polymer solution, free of unacetylated ceUulose, rigid particle contaminants, and dirt, must pass through spinnerets with holes of 30—80 ]lni diameter. Multistage filtration, usuaUy through plate-and-frame filter presses with fabric and paper filter media, removes the extraneous matter before extmsion. Undesirable gelatinous particles, such as the hemiceUulose acetates from ceUulose impurities, tend to be sheared into smaller particles rather than removed. The solution is also aUowed to degas in hoi ding tanks after each state of filtration. [Pg.296]

The principle of solvent extraction in refining is as follows when a dilute aqueous metal solution is contacted with a suitable extractant, often an amine or oxime, dissolved in a water-immiscible organic solvent, the metal ion is complexed by the extractant and becomes preferentially soluble in the organic phase. The organic and aqueous phases are then separated. By adding another aqueous component, the metal ions can be stripped back into the aqueous phase and hence recovered. Upon the identification of suitable extractants, and using a multistage process, solvent extraction can be used to extract individual metals from a mixture. [Pg.168]

Continuous production of urea—formaldehyde resins has been described in many patents. In a typical example, urea and formaldehyde are combined and the solution pumped through a multistage unit. Temperature and pH are controlled at each stage to achieve the appropriate degree of polymerization. The product is then concentrated in a continuous evaporator to about 60—65% soflds (31). [Pg.326]

Cyclohexanone oxime is converted quantitatively to caprolactam by Beckmann rearrangement in the presence of oleum, which is of sufficient strength to consume the several percent water in the molten oxime. The reaction mass is neutralized with aqueous ammonia to a cmde caprolactam layer and a saturated solution of ammonium sulfate. Approximately 1.5 kg of the total 4.4 kg ammonium sulfate per kilogram of caprolactam is produced in this step. Purification is by multistage vacuum crystallization from aqueous solution in neatly quantitative yield. [Pg.429]

Availability of large digital computers has made possible rigorous solutions of equilibrium-stage models for multicomponent, multistage distillation-type columns to an exactness limited only by the accuracy of the phase equilibrium and enthalpy data utilized. Time and cost requirements for obtaining such solutions are very low compared with the cost of manual solutions. Methods are available that can accurately solve almost any type of distillation-type problem quickly and efficiently. The material presented here covers, in some... [Pg.1277]

Multicomponent systems containing four or more components become difficult to display graphically. However, process-design calculations can often be made for the extraction of the component with the lowest partition ratio K and treated as a ternaiy system. The components with higher K values may be extracted more thoroughly from the raffinate than the solute chosen for design. Or computer calculations can be used to reduce the tedium of multicomponent, multistage calculations. [Pg.1451]

Multistage counter-current liquid-liquid extraction is a typical continuous process. Fig. 121 shows a schematic diagram of the process. The slope of the line depends on the volumetric ratio of the aqueous and organic phases. The aqueous and organic phases move through the system as two counter currents. The raffinate from a specific extraction stage moves on to the next stage, to be mixed with a relatively fresh portion of the extract, i.e. extractant that was previously mixed with a low-concentration aqueous solution. [Pg.272]

Several attempts were made to apply nanostructures made of DNA or proteins to the development of alternative computation or computer memory. The concept of DNA computing was developed as an alternative computation approach based on information and data stored as sequenced DNA nucleotides and DNA-specific hybridization and elongation as a means to reach the answer or solution to a problem. Available tools of molecular biology were employed to identify and analyze the results [66-68]. This multistage computation is based on the assumption that solutions can be sought in parallel, thus compensating for the relatively slow processing time. [Pg.468]

Although more complex in form, the resulting model equations provide no major additional difficulty, and solution is also easily obtained. Multistage extraction with backmixing is covered in the simulation example EQBACK. [Pg.179]

Dynantics of Heat Exchangers, Simple Batch Extraction, Multi-Solute Batch Extraction, Multistage Countercurrent Ctiscade, Extraction Cascade with Backmixing, Countercurrent Extraction Cascade with Reaction, Absorption with Chemical Reaction, Membrane Transfer Processes... [Pg.722]

An infinitely large volume of solvent is needed to achieve complete extraction of a solute in a single stage. This necessitates application of multistage extraction. It allows essentially complete recovery deploying a limited volume of the solvent. In the countercurrent proc-... [Pg.518]

The sample volume initially introduced onto the sorbent, the choice of sorbent and solvent system and careful control of the amount of solvent used are of paramount importance for effective pre-concentration and/or clean-up of the analyte in the sample. The number of theoretical plates in an SPE column is low (/V = 10-25). SPE is a multistage separation method and as such requires only a reasonable difference in extractability to separate two solutes. In SPE concentration factors of 1000 or more are possible, as compared to up to 100 for LLE with vortex mixing. [Pg.125]

Smith and Brinkley developed a method for determining the distribution of components in multicomponent separation processes. Their method is based on the solution of the finite-difference equations that can be written for multistage separation processes, and can be used for extraction and absorption processes, as well as distillation. Only the equations for distillation will be given here. The derivation of the equations is given by Smith and Brinkley (1960) and Smith (1963). For any component i (suffix i omitted in the equation for clarity)... [Pg.522]

Rose et al. (1958) and Hanson and Sommerville (1963) have applied relaxation methods to the solution of the unsteady-state equations to obtain the steady-state values. The application of this method to the design of multistage columns is described by Hanson and Sommerville (1963). They give a program listing and worked examples for a distillation column with side-streams, and for a reboiled absorber. [Pg.545]

In this section, the TA-based modeling and solution approach is applied to a popular benchmark scheduling problem from Kallrath [1], It is a multistage and multiproduct chemical batch plant. [Pg.229]

Figure 14.11 Basis for graphical solution for multistage CSTR (for A +. .. - products)... Figure 14.11 Basis for graphical solution for multistage CSTR (for A +. .. - products)...
Assuming the liquid phases remain immiscible, the modelling approach for multicomponent systems remains the same, except that it is now necessary to write additional component balance equations for each of the solutes present, as for the multistage extraction cascade with backmixing in Section 3.2.2. Thus for component j, the component balance equations become... [Pg.140]


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See also in sourсe #XX -- [ Pg.487 ]




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