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Solvent classification general

Solvent classification In acid-base reactions the solvent plays an active or specific role in two ways it may react generally with ions and molecules (solvation), and as indicated above, it has acidic and basic properties that are of active concern. Broadly, solute-solvent interactions are studied by electrical and spectral methods. ... [Pg.63]

The Snyder solvent classification scheme (29, 30) that has been successfully applied to LC systems (31-37) for LC separation optimization appears to be a general framework that can be used for guidance in the selection of the modifier. Some preliminary experiments have been done to determine the applicability of this approach to SFC systems as a prelude to a more in-depth, statistically-designed modifier selection study. These first experiments are the topic of this paper the basis of the proposed modifier selection scheme will now be described in detail. [Pg.146]

A review of the selected definitions suggests that there are many important determinants of solvent quality for specific apphcation. Some solvent parameters are conflicting, some not well quantified, and each solvent application requires a unique set of solvent performance criteria. It can be thus anticipated, prior to any analysis, that the chemical structure can be used as the best means of solvent classification for any application. Such a classification is used in this book because of its broad application. Chemical names used are the common names beeause they are generally understood by all solvents users. [Pg.69]

The products could be classified as a function of various criteria physical properties (in particular, volatility), the way they are created (primary distillation or conversion). Nevertheless, the classification most relevant to this discussion is linked to the end product use LPG, premium gasoline, kerosene and diesel oil, medium and heavy fuels, specialty products like solvents, lubricants, and asphalts. Indeed, the product specifications are generally related to the end use. Traditionally, they have to do with specific properties octane number for premium gasoline, cetane number for diesel oil as well as overall physical properties such as density, distillation curves and viscosity. [Pg.483]

This classification is concerned with whether the detector responds to a specific feature of the analyte of interest or whether it will respond to a large number of analytes, irrespective of their structural properties. In terms of the previous classification, it may be considered that solute detectors are also usually selective detectors, while solvent detectors are general detectors. [Pg.33]

Defoamer formulations currently contain numerous ingredients to meet the diverse requirements for which they are formulated. Various classification approaches are possible, including classification by application, physical form of the defoamer, and the chemical type of the defoamer. In general, defoamers contain a variety of active ingredients, both in solid and in liquid states, and a number of ancillary agents such as emulsifiers, spreading agents, thickeners, preservatives, carrier oils, compatibilizers, solvents, and water. [Pg.317]

From our previous treatment of the Arrhenius, Bransted and Lewis acid-base theories, the importance of the choice between the divergent solvent types clearly appeared if we now confine ourselves to solvents to which the proton theory in general is applicable, this leads to a classification of eight classes as already proposed by Bronsted35,36 (Table 4.3). [Pg.268]

This is the most common route, the reagent being a metal compound/solvent combination. Typical conditions call for the metal salt (e.g., acetate) in a buffer system (e.g., NaOAc/AcOH) and a co-solvent such as chloroform. Generally the reaction mixture is refluxed until the metal complex spectrum (see Section 9.22.5.6 and Table 4) is fully developed. Metal acetylacetonates and metal phenoxides have also been employed. The topic has been reviewed in detail by Buchler,51 who has also summarized the history and classification of metal complexes of this series, and the mechanisms of metalation.52... [Pg.955]

Intramolecular general base catalysed reactions (Section II, Tables E-G) present less difficulty. A classification similar to that of Table I is used, but since the electrophilic centre of interest is always a proton substantial differences between different general bases are not expected. This section (unlike Section I, which contains exclusively unimolecular reactions) contains mostly bimolecular reactions (e.g. the hydrolysis of aspirin [4]). Where these are hydrolysis reactions, calculation of the EM still involves comparison of a first order with a second order rate constant, because the order with respect to solvent is not measurable. The intermolecular processes involved are in fact termolecular reactions (e.g. [5]), and in those cases where solvent is not involved directly in the reaction, as in the general base catalysed aminolysis of esters, the calculation of the EM requires the comparison of second and third order rate constants. [Pg.223]

Residual solvents are the third general classification of impurities in pharmaceuticals. This class is described as inorganic or organic liquids used during the manufacturing process. Typically, these solvents can only be evaluated by gas chromatography and therefore will not be addressed in this chapter. [Pg.362]

Classification by Chemical Constitution Classification of solvents according to chemical constitntion allows certain qualitative predictions. In general, a compound dissolves far more easily in a solvent possessing related functional groups than in one of a completely different nature (see table 3.11). A proper choice of solvent, based on the knowledge of its chemical reactivity, helps to avoid undesired reactions between solute and solvent. [Pg.69]

The three general classifications of acid-gas removal processes are 1) amines, 2) activated hot potassium carbonate, and 3) physical solvents. These systems each have preferred operating ranges, as generally controlled by the acid-gas partial pressure, have different energy requirements, and offer different degrees of selectivity. [Pg.28]


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