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Adsorptive separations

Fig. 8. UOP Parex simulated moving bed for adsorptive separation. AC = adsorbent chamber RV = rotary valve EC = extract column ... Fig. 8. UOP Parex simulated moving bed for adsorptive separation. AC = adsorbent chamber RV = rotary valve EC = extract column ...
In contrast to trace impurity removal, the use of adsorption for bulk separation in the liquid phase on a commercial scale is a relatively recent development. The first commercial operation occurred in 1964 with the advent of the UOP Molex process for recovery of high purity / -paraffins (6—8). Since that time, bulk adsorptive separation of liquids has been used to solve a broad range of problems, including individual isomer separations and class separations. The commercial availability of synthetic molecular sieves and ion-exchange resins and the development of novel process concepts have been the two significant factors in the success of these processes. This article is devoted mainly to the theory and operation of these Hquid-phase bulk adsorptive separation processes. [Pg.291]

Since 1971 mainly adsorptive separation processes are used to obtain high purity -xylene (55,84—86). A typical commercial process for the separation of -xylene from other Cg aromatics produces about 99.8% purity -xylene at greater than 95% recovery. [Pg.300]

Aromatic and Nonaromatic Hydrocarbon Separation. Aromatics are partially removed from kerosines and jet fuels to improve smoke point and burning characteristics. This removal is commonly accompHshed by hydroprocessing, but can also be achieved by Hquid-Hquid extraction with solvents, such as furfural, or by adsorptive separation. Table 7 shows the results of a simulated moving-bed pilot-plant test using siHca gel adsorbent and feedstock components mainly in the C q—range. The extent of extraction does not vary gready for each of the various species of aromatics present. SiHca gel tends to extract all aromatics from nonaromatics (89). [Pg.300]

A surprisiagly large number of important iadustrial-scale separations can be accompHshed with the relatively small number of zeoHtes that are commercially available. The discovery, characterization, and commercial availabiHty of new zeoHtes and molecular sieves are likely to multiply the number of potential solutions to separation problems. A wider variety of pore diameters, pore geometries, and hydrophobicity ia new zeoHtes and molecular sieves as weU as more precise control of composition and crystallinity ia existing zeoHtes will help to broaden the appHcations for adsorptive separations and likely lead to improvements ia separations that are currently ia commercial practice. [Pg.303]

The value of many chemical products, from pesticides to pharmaceuticals to high performance polymers, is based on unique properties of a particular isomer from which the product is ultimately derived. Eor example, trisubstituted aromatics may have as many as 10 possible geometric isomers whose ratio ia the mixture is determined by equiHbrium. Often the purity requirement for the desired product iacludes an upper limit on the content of one or more of the other isomers. This separation problem is a compHcated one, but one ia which adsorptive separation processes offer the greatest chances for success. [Pg.303]

Fig. 12. Classification of adsorptive separations where NG = natural gas and S = sulfur. Fig. 12. Classification of adsorptive separations where NG = natural gas and S = sulfur.
BulkSepa.ra.tlon, The adsorptive separation of process streams into two or more main components is termed bulk separation (see Fig. 12). The development of processes and products is complex. Consequently, these processes are proprietary and are purchased as a complete package under licensing agreements. High purities and yields can be achieved. [Pg.457]

These mechanisms are characterized by the relative magnitudes of the heats of reaction, solution, or adsorption (see Adsorption, separation). AH useflil drying mechanisms are exothermic. Phosphoms pentoxide is a Class 1 drying agent that reacts with water to form a polyphosphoric acid (2) ... [Pg.505]

Clinoptilolite is microporous crystalline solid with well-defined structure, which have great potential for a number of applications in various fields, such as adsorption, separation, ion-exchange and catalysis. [Pg.255]

Apart from such trough chambers there are also S-chamber systems (small chambers, sandwich chambers) with deliberately reduced vapor volumes, which are specially suited to adsorptive separations. Such chambers are available for vertical and horizontal development (Fig. 58). Different separation results are naturally obtained in trough and S-chambers [8]. [Pg.126]

Ruthven D. M., Ching C. B. (1989) Counter-Current and Simulated Counter-Current Adsorption Separation Proeesses, Chem. Eng. Sci. 44 1011-1038. [Pg.251]

Storti G., Mazzotti M., Morbidelli M., Carra S. (1993) Robust Design of Binary Countereurrent Adsorption Separation Proeesses, AIChEJ. 39 471-492. [Pg.251]

Because p-xylene is the most valuable isomer for producing synthetic fibers, it is usually recovered from the xylene mixture. Fractional crystallization used to be the method for separating the isomers, but the yield was only 60%. Currently, industry uses continuous liquid-phase adsorption separation processes.The overall yield of p-xylene is increased... [Pg.39]

FIG. 4 Sorbex-simulated bed for adsorptive separation. AC, adsorbent chamber RV, rotary valve EC, extract column RC, raffinate column. (From Ref. 32.)... [Pg.49]

The search for adsorptive applications of MOFs has up to now mainly focused on the storage of small molecules in gas phase, for instance, H2, CO2, CH4, or NO [46, 92, 93]. This section focuses on the application of MOFs for adsorptive separation of larger molecules and in the hquid phase, a domain in which their potential only recently has been recognized (Figure 4.3). [Pg.86]

Regardless of the location of the protein and its state, cell separation needs to be inemensive, simple, and reliable, as large amounts of fermentation-broth dilute in the desired product may be handled. The objectives are to obtain a well-clarified supernatant and solids of maximum dryness, avoiding contamination by using a contained operation. Centrifugation or crossflow filtration is t ically used for cell separation, and both unit operations can be run in a continuous-flow mode [Datar and Rosen, in Stephanopoulos (ed.), op. cit., pp. 369-503]. In recent years, e3q>anded-bea adsorption has become an alternative. It combines broth clarification and adsorption separation in a single step. [Pg.73]


See other pages where Adsorptive separations is mentioned: [Pg.19]    [Pg.19]    [Pg.19]    [Pg.251]    [Pg.251]    [Pg.266]    [Pg.268]    [Pg.269]    [Pg.269]    [Pg.282]    [Pg.288]    [Pg.295]    [Pg.299]    [Pg.303]    [Pg.306]    [Pg.459]    [Pg.449]    [Pg.478]    [Pg.483]    [Pg.1555]    [Pg.2063]    [Pg.10]    [Pg.251]    [Pg.73]    [Pg.427]    [Pg.427]    [Pg.80]    [Pg.80]   
See also in sourсe #XX -- [ Pg.50 ]




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Adsorption chromatographic separations

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Adsorption effects, separation

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Adsorptive bubble separation

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