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Separating tools

By the time the next overview of electrical properties of polymers was published (Blythe 1979), besides a detailed treatment of dielectric properties it included a chapter on conduction, both ionic and electronic. To take ionic conduction first, ion-exchange membranes as separation tools for electrolytes go back a long way historically, to the beginning of the twentieth century a polymeric membrane semipermeable to ions was first used in 1950 for the desalination of water (Jusa and McRae 1950). This kind of membrane is surveyed in detail by Strathmann (1994). Much more recently, highly developed polymeric membranes began to be used as electrolytes for experimental rechargeable batteries and, with particular success, for fuel cells. This important use is further discussed in Chapter 11. [Pg.333]

Even though it appears that the technology has not been adopted yet, it is expected that TOE MS will be useful to validate the power of the GC X GC separation experiment by proving the separate identities of the vast number of resolved peaks and so show that the analyst who does not use GC X GC is missing valuable chemical compositional information on their samples. In addition, it is just as significant to TOEMS that GC X GC becomes a widespread separation tool, since this will then provide a demand for the powerful capabilities of TOEMS for identification. The GC community must wait for this to be demonstrated, and those who are working in GC X GC development are convinced that the wait will be worth it ... [Pg.105]

E. Erancotte, Chromatography as a separation tool for the preparative resolution of racemic compounds in Chiral separations, applications and technology, S. Ahuja (Ed.), American Chemical Society, Washington (1997) Chapter 10. [Pg.19]

Erancotte E. (1996) Chromatography as a Separation Tool for the Preparative Resolution of Racemic Compounds, in Chiral Separations. Applications and Technology, Ahuja S. (ed.), American Chemical Society, p. 271-308. [Pg.250]

Here is the first book devoted completely to inorganic membrane separations and applications. It provides detailed information on all aspects of the development and utilization of both commercial and developmental inorganic membranes and membrano-t)ased processes, pointing out their key advantages and limitations as separation tools. [Pg.150]

As documented in Chapter 5, zeolites are very powerful adsorbents used to separate many products from industrial process steams. In many cases, adsorption is the only separation tool when other conventional separation techniques such as distillation, extraction, membranes, crystallization and absorption are not applicable. For example, adsorption is the only process that can separate a mixture of C10-C14 olefins from a mixture of C10-C14 hydrocarbons. It has also been found that in certain processes, adsorption has many technological and economical advantages over conventional processes. This was seen, for example, when the separation of m-xylene from other Cg-aromatics by the HF-BF3 extraction process was replaced by adsorption using the UOP MX Sorbex process. Although zeolite separations have many advantages, there are some disadvantages such as complexity in the separation chemistry and the need to recover and recycle desorbents. [Pg.203]

Adsorptive separation is a powerful technology in industrial separations. In many cases, adsorption is the only technology available to separate products from industrial process streams when other conventional separation tools fail, such as distillation, absorption, membrane, crystallization and extraction. Itis also demonstrated that zeolites are unique as an adsorbent in adsorptive separation processes. This is because zeolites are crystalline soUds that are composed of many framework structures. Zeolites also have uniform pore openings, ion exchange abiUty and a variety of chemical compositions and crystal particle sizes. With the features mentioned, the degree of zeoUte adsorption is almost infinite. It is also noted that because of the unique characteristics of zeoHtes, such as various pore openings, chemical compositions and structures, many adsorption mechanisms are in existence and are practiced commercially. [Pg.225]

Although CE has been developed as a separation tool, it has quite useful characteristics for measuring the physicochemical properties of drugs with higher throughput and lower sample consumption in comparison with conventional methods. With the recent advances in combinatorial chemistry and in vitro pharmacological assay, rapid and reliable analytical methods for physicochemical parameter measurement are required to accelerate the drug... [Pg.79]

The principal types of industrial adsorbent can be divided into amorphous and the crystalline types. The former includes activated carbon, silica gel, and activated alumina the latter includes zeolites and their aluminum phosphate, AIPO4 (or ALPO), analogs. Yang (2003) wrote that, since the invention of synthetic zeolites in 1959, adsorption has become a key separation tool in the chemical, petrochemical, and pharmaceutical industries. Adsorptive separation of different molecules can be achieved by three mechanisms equilibrium adsorption differences, diffusion kinetics differences. [Pg.321]

Others FFF techniques, such as Acoustical FFF and Dielectric FFF are promising separation tools but they have not yet reached the commercial stage. Interested readers should address to specific literature [3]. [Pg.356]

Remember HPLC is a versatile, powerful, but basically simple separation tool. It is a time machine that can speed your research and, thereby, allow you to do many things not possible with slower techniques. It is both an analytical and a preparative machine. When I finish, I hope you will have the confidence to run your instrument, make your own mistakes, and be able to find your own solutions. [Pg.2]

The two-dimensional techniques, both as a preparative tool for collecting fractions and perhaps especially as a separative tool in rapid star electrophoresis, will undoubtedly prove to be of great value in clinical laboratory work. The recent technical improvements in the apparatus allow for easy working conditions. These were previously lacking and delayed the clinical use of methods which are based on a different principle from that of zone electrophoresis. They yield important results in fields where the one-dimensional method has partly failed. [Pg.120]

The subject has been extensively studied by Rebek and coworkers, who have written a substantial number of reviews covering different aspects of the topic [45]. Because of this, we do not intend to describe here in detail the different systems that have been developed, but focus instead on some of the dynamic aspects. Possible applications of these systems include molecular containers, enantioselec-tive receptors, catalysts, drug-delivery devices, separation tools or simply unusual... [Pg.91]

Ultrafiltration, which uses selective membranes to separate materials on the basis of different molecular sizes, has become a valuable separation tool for a wide variety of industrial processes, particularly in the separation of dispersed colloids or suspended solids. In many cases where a high degree of separation is desired, a batch ultrafiltration process is used because it is the most economical in terms of membrane area. [Pg.448]

The International Union of Pure and Applied Chemistry (IUPAC) recommends the use of liquid-liquid distribution rather than the traditional term, solvent extraction. However, solvent extraction is still used commonly in the literature, and that is why it is also being used here interchangeably (Chapter 7). Solvent extraction utilizes the partition of a solute between two practically immiscible liquid phases—one a solvent phase and the other an aqueous phase. Liquid-liquid partitioning methods are important separation tools in modern biotechnology. They have become increasingly popular as part of a... [Pg.9]

The feedstock from which the antibodies are to be extracted dictates the choice of the separation tools and to some extent the sequence of the chromatographic columns (see Section V.I). [Pg.547]


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See also in sourсe #XX -- [ Pg.173 ]




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